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1 V1 and RL.SIGNIFICANCE STATEMENT A major cue for inferring 3D depth is disparity between the two eyes
2  sampling of the parameter space is critical for inferring a correct model structure.
3 llenges, we present a novel algorithm DLCpar for inferring a most parsimonious (MP) history of a gene
4 diversity, but this is nonetheless essential for inferring accurately the history of species with ove
5 ms originate from the motor system and allow for inferring actions from environmental affordances, an
6                              Many approaches for inferring adaptive molecular evolution analyze the u
7 ion concern, and provide a general framework for inferring allele distribution and persistence and in
8 ve methods for estimating site allele count, for inferring allele frequency spectrum and for associat
9                     The rate limiting factor for inferring an association between a variant and a phe
10                      We present an algorithm for inferring ancestry segments and characterizing admix
11 results and developing computational methods for inferring and analyzing these networks.
12 ple algorithms provide a stronger foundation for inferring and characterizing regulatory programs ass
13                          We present a method for inferring and constructing transport reactions for t
14 le feedback pathways that provide mechanisms for inferring and interpreting what sensory inputs are a
15                  (2020) present an algorithm for inferring and inverting such trial-to-trial differen
16  and discuss a suite of algorithms and tools for inferring and scoring regulator networks upstream of
17       Mitochondrial genomes have been useful for inferring animal phylogeny across a wide range of cl
18                 This resource will be useful for inferring bacterial gene function and provides a dra
19         We apply the joint modeling approach for inferring base pairing states on simulated data sets
20 These findings establish Collage as a method for inferring biological knowledge from the integration
21 Sparse Gaussian graphical models are popular for inferring biological networks, such as gene regulato
22 ck size estimates, we introduce a new method for inferring bottleneck sizes that accounts for these f
23                  Here we present a framework for inferring cancer-related gene overexpression resulti
24 P method quantifies confidence probabilities for inferring causal structures and thus leads to more r
25 lities, ScisTree implements a fast heuristic for inferring cell lineage tree and calling the genotype
26 ontent of our repository, provide procedures for inferring cell-cell communication networks from sing
27 r of estimated cell types are critical steps for inferring cell-type proportions.
28                          We developed a tool for inferring cellular architectures across many domains
29 ining, making V. monoica a suitable outgroup for inferring changes in papaya sex chromosomes.
30 a method, similar to regression calibration, for inferring changes in the distribution of white blood
31 od based on water mass transformation theory for inferring changes in the water cycle from changes in
32  Here, we present a new method, CloneSeeker, for inferring clinical heterogeneity from sequencing dat
33 seq) technologies produce data that is ideal for inferring CNAs.
34  integer copy number, few have been designed for inferring CNV haplotypic phase and none of these are
35 es, predicting CNV allelic configuration and for inferring CNV haplotypic phase from SNP/CNV genotype
36  of genome-scale data can serve as the basis for inferring combinatorial regulation and for building
37 raph diffusion kernel as a unified framework for inferring complex/pathway membership analogous to "f
38 NP-SEQ is a statistical model-based approach for inferring copy number profiles directly from high-co
39 arkov Models (HMM) to analyze SNP array data for inferring copy numbers and loss-of-heterozygosity (L
40    Although there are many methods available for inferring copy-number variants (CNVs) from next-gene
41 OV) which combines three distinct approaches for inferring covariation signals from multiple sequence
42  we demonstrate the usefulness of the method for inferring demographic history, especially recent cha
43     We propose a hierarchical Bayesian model for inferring differences between groups of samples more
44 the existence of many programs and databases for inferring different protein functions, a pipeline th
45             Here we present a general method for inferring direct effects from an observed correlatio
46 only validate our widely-applicable approach for inferring directed genotype networks from data, but
47 fers to a family of computational techniques for inferring disease genes through a set of training ge
48 xplanation space to be particularly valuable for inferring disease subtypes, the method is more gener
49  These detailed data have been proven useful for inferring disease transmission to a more refined lev
50    mirConnX is a user-friendly web interface for inferring, displaying and parsing mRNA and microRNA
51                Here we introduce a framework for inferring DNA-binding specificities by considering p
52                                      Methods for inferring dominance hierarchies are relatively robus
53     We present MDSINE, a suite of algorithms for inferring dynamical systems models from microbiome t
54                We then describe a new method for inferring each individual's germline gene set from d
55           We propose MCM as a novel approach for inferring EC from neuronal energy metabolism that is
56 ance of quantitative seasonal abundance data for inferring ecological distributions and demonstrate s
57 dy, we test the suitability of these methods for inferring ecological interactions by constructing ne
58                 Here we describe a procedure for inferring eye position using multi-electrode array r
59                         Conventional methods for inferring FOI estimate a time-averaged value and are
60                                 Thus methods for inferring [Formula: see text] and the degree of hete
61                  This has broad implications for inferring function from the presence of structurally
62 er 2/3 pyramidal neurons to validate methods for inferring functional connectivity in a setting where
63           We compare phylogenetic approaches for inferring functional gene links.
64 irst is a computationally inexpensive method for inferring functional information from protein crysta
65                 We describe a novel approach for inferring functional relationship of proteins by det
66                The database can also be used for inferring functionality, which for membrane proteins
67 ted parsimony and maximum likelihood methods for inferring gain and loss events.
68 ssociated genes, better than popular methods for inferring gene expression networks.
69 ns, and (3) developed an efficient algorithm for inferring gene expression rate constants from the mo
70 itance, operon and gene fusion-based methods for inferring gene function and reconstructing cellular
71  genetic screens provide a powerful approach for inferring gene function on the basis of the phenotyp
72 , we present GINI, a machine learning system for inferring gene interaction networks from Drosophila
73 ntal data are a valuable, but limited source for inferring gene regulation mechanisms on a genomic sc
74 ic evaluation of state-of-the-art algorithms for inferring gene regulatory networks from single-cell
75 ing of transcriptional regulation as well as for inferring gene regulatory networks.
76 propose an improved gene clustering approach for inferring gene signaling pathways from gene microarr
77                                 Most methods for inferring gene-gene interactions from expression dat
78 he differences that do exist are informative for inferring general principles about the holistic evol
79 efrontal cortex (VMPFC) activation increased for inferring generous play and decreased for inferring
80 ful for identifying an appropriate technique for inferring genetic networks and for interpreting the
81   We have developed and implemented a method for inferring genetic regulatory networks for time serie
82  approach is a model-based imputation method for inferring genotypes at observed or unobserved SNPs,
83 ly Bayesian approaches (originally developed for inferring geographic spread and rates of molecular e
84 ications for sawfish conservation as well as for inferring habitat residency of euryhaline elasmobran
85 ently selected alleles, eliminating the need for inferring haplotype.
86  three previously published Bayesian methods for inferring haplotypes from genotype data in a populat
87 we believe that polyHap, our proposed method for inferring haplotypic phase from genotype data, will
88 an overgeneralization of adaptive mechanisms for inferring harmful intentions and the ability to caus
89                      We present a new method for inferring hidden Markov models from noisy time seque
90          Here we present a general technique for inferring hierarchical structure from network data a
91                       There are many methods for inferring hierarchies from social interactions.
92 archy affect the performance of five methods for inferring hierarchies, (2) propose an amendment that
93                  EBEN provides a useful tool for inferring high-dimensional sparse model in multiple
94 on penalties in the most widely used methods for inferring homology by sequence alignment, including
95    Our model improves on previous approaches for inferring host mortality from parasite abundance dat
96      Our results illustrate a general method for inferring how groups of neurons work together to mod
97                  These results may be useful for inferring how thermal alteration of soil by wildfire
98 d assessed multiple computational approaches for inferring human biology from mouse datasets.
99  technology has provided a great opportunity for inferring human demographic history by investigating
100  macrophage model of infection is unsuitable for inferring human-relevant differences in nontyphoidal
101            As genetic datasets grow, methods for inferring IBD segments that scale well will be criti
102 as well as in defining computational methods for inferring (imputing) unknown interactions.
103                  We present a novel approach for inferring influence of a rare stressor on a rare spe
104 rdiffusive motion, is of particular interest for inferring information about the dynamics of the cyto
105 ids was recently introduced as a useful tool for inferring information on such correlated sites.
106 but although many methods have been proposed for inferring integer copy number, few have been designe
107 e capacity for curiosity and exploration and for inferring internal models of the external world.
108 , we present OncoNEM, a probabilistic method for inferring intra-tumor evolutionary lineage trees fro
109 ch as approximate Bayesian computation (ABC) for inferring invasion history.
110 on of a protein has become a useful practice for inferring its function.
111 dysregulation and has important implications for inferring ketamine's mechanism of action from studie
112 o (semi)-unsupervised data-driven approaches for inferring latent structures that may give insight in
113              Furthermore, we propose methods for inferring LD-decay rates and recombination hotspots
114 applying CIBERSORT, a computational approach for inferring leukocyte representation in bulk tumor tra
115 s them in a single report, which can be used for inferring likely causal genes.
116         Many software packages are available for inferring local ancestry in admixed individuals.
117    We present a new haplotype-based approach for inferring local genetic ancestry of individuals in a
118 MAP, ancestry of Modern Admixed Populations) for inferring local phased ancestry.
119 population and subsequently develop a method for inferring location to a finer scale.
120 ogeneous Bayesian analysis of variance model for inferring loci involved in recent selective sweeps b
121 ate and more efficient than existing methods for inferring locus-specific ancestries, enabling it to
122 working clinician and their predictive power for inferring long term viral eradication from short ter
123 hlights contagion maps also as a viable tool for inferring low-dimensional structure in networks.
124 pproach is the use of computational modeling for inferring mechanisms which generate observed behavio
125 trol methods, and provides a powerful method for inferring mechanistic relationships underlying biolo
126 moother procedure provides a powerful method for inferring melt rates in a warming world.
127 em (MNS) and some a mentalizing system (MZS) for inferring mental states.
128 tudies of Buchnera have provided a new means for inferring metabolic capabilities of the symbionts an
129 easuring macro- and mesoscopic structure and for inferring microstructural properties; we also descri
130           Admixed populations have been used for inferring migrations, detecting natural selection, a
131                    Here, we present a method for inferring missing CNV genotypes, predicting CNV alle
132                       We propose a framework for inferring models of tumor progression from single-ce
133   Quantitative microscopy is a valuable tool for inferring molecular mechanisms of cellular processes
134                                 Implications for inferring molecular mechanisms of solvent effects on
135 e developed an integrated, scalable strategy for inferring multiple human gene interaction types that
136                          We present a method for inferring mutation and gene-conversion rates by usin
137 velop a novel Bayesian statistical framework for inferring natural selection at a pair of linked loci
138  3D genome which may provide key information for inferring neoantigens' immunogenicity.
139 werful experimental-computational technology for inferring network models that predict the response o
140 ruction of large networks, we developed Tool for Inferring Network of Genes (TINGe), a parallel mutua
141 rrelational methods are increasingly popular for inferring networks from co-occurrence and time serie
142 optical signals have yielded various metrics for inferring neural connectivity, and hence for mapping
143  (P <10(-4)), properties that were important for inferring new candidate interactions.
144 principle demonstration of a novel framework for inferring, noninvasively, neuromodulatory influences
145                  Although several algorithms for inferring nucleosome position from a single experime
146                        It also proves useful for inferring numbers of secondary infections and identi
147                          One useful strategy for inferring others' mental states (i.e., mentalizing)
148                          Statistical methods for inferring parameters such as the recombination rate
149                                While methods for inferring parental haplotype assignments on large F1
150 ause it has been shown that they can be used for inferring participation in a study if the individual
151                  However, current approaches for inferring past migration episodes in the fields of a
152                    We present a novel method for inferring patient-specific genetic activities incorp
153         We propose a computational framework for inferring phenotypic crosstalk (PHOCOS) that is suit
154 ggesting that these loci are not appropriate for inferring phylogenetic relationships among species.
155 ere, we present a novel computational method for inferring phylogenetic relationships from partial se
156              We present a statistical method for inferring phylogenetic trees from EST-based incomple
157 termining the molecular basis of adaptation, for inferring phylogenies and for engineering novel prot
158 sure and fast running time make MulRF useful for inferring phylogenies from large collections of gene
159 o propose a natural graphical representation for inferring phylogenies.
160 esent a principled likelihood-based approach for inferring physical models of TF-DNA binding energy f
161 ially offer a powerful statistical framework for inferring population genetic parameters.
162  led to the development of new methodologies for inferring population history and refuelled the debat
163 dicate that the modified SG method is useful for inferring positive selection at codon sites where ne
164 terns to identify spatially similar patterns for inferring potential genetic interactions.
165                            A web application for inferring potentially stabilizing non-bonding intera
166                These results are fundamental for inferring processes on Earth and other planets from
167 understanding the dynamics of adaptation and for inferring properties of an organism's fitness landsc
168                    A large literature exists for inferring/proposing biological pathways/networks usi
169                      We present an algorithm for inferring protein complexes from weighted interactio
170 into ProDy, a computational toolbox designed for inferring protein dynamics from experimental and the
171 ervation is an important, established method for inferring protein function, modularity and specifici
172 arities between proteins is often unreliable for inferring protein function.
173 in subcellular localization is indispensable for inferring protein functions.
174 the usefulness of order/disorder predictions for inferring protein structure from sequence.
175            Molecular biomarkers hold promise for inferring rates of key metabolic activities in compl
176                Current estimation techniques for inferring reaction rates frequently rely on marginal
177 n widely applied population genetics methods for inferring recombination rates, for detecting selecti
178 SHUS, that implements three exact algorithms for inferring regions of hemizygosity containing genomic
179  In this paper, we present a novel framework for inferring regulatory and sequence-level information
180              Based on our empirical criteria for inferring regulatory effects (presence-absence of sp
181 h motifs in genome sequences is a major goal for inferring regulatory networks yet has been hampered
182 e basal tracheophyte genome, which is useful for inferring relationships among bryophyte lineages.
183 to stimulate development of analytical tools for inferring relationships between somatic changes and
184 actions (i.e. sampling effort) are necessary for inferring reliable dominance hierarchies, nor are th
185       We present a maximum likelihood method for inferring reticulate evolutionary histories while ac
186 monstrate that BIC provides a good framework for inferring reticulate evolutionary histories.
187 tic variants as valid instrumental variables for inferring risk factors causing coronary artery disea
188 t software implementing a model-based method for inferring ROH in genome-wide SNP datasets that incor
189            DupTree is a new software program for inferring rooted species trees from collections of g
190 ocessing are of interest to forensic science for inferring sample provenance.
191 y, we discuss challenges and recommendations for inferring selection on introgressed regions.
192 ed for inferring generous play and decreased for inferring selfish play.
193                     Here we propose a method for inferring sets of biochemical rate constants that go
194 nt DyStruct, a model and inference algorithm for inferring shared ancestry from temporally sampled ge
195 ession for Signaling Determination (DESIDE), for inferring signaling activity from microarray measure
196                A variety of techniques exist for inferring signaling pathways.
197 p and protein modification are indispensable for inferring signalling pathways from PPI networks.
198 ween protein sequences that can be important for inferring similarity of structure or function.
199 ch techniques demonstrate high success rates for inferring 'simple' genomic segments, they are confou
200 cleotide substitutions, a learning algorithm for inferring site-specific substitution biases directly
201             The proposed framework is useful for inferring small NM-based modules of TF-target gene r
202              We discuss different approaches for inferring social networks from these data and displa
203                    Here, we develop a method for inferring some aspects of the order of mutational ev
204 C) model has emerged as a powerful framework for inferring species phylogenies while accounting for a
205 ing species tress) is a new software package for inferring species trees while accommodating uncertai
206 ifying downstream snapshot measures required for inferring specific dynamical features of upstream si
207       We derive a general Bayesian framework for inferring statistically optimized atomic potentials
208 unodeficiency virus type 1 (HIV-1) is useful for inferring structural and/or functional constraints a
209 tumor Evolution), a new probabilistic method for inferring subclonal history and lineage tree reconst
210                  Recently, tools and methods for inferring such gene sequences from AIRR-seq datasets
211         Here, we present a general framework for inferring such histories and demonstrate how it can
212          We propose a new algorithmic method for inferring such interactions between genes using data
213 ding influences gene expression is important for inferring target genes from TF chromatin immunopreci
214          We present a new tool, PAREameters, for inferring targeting criteria from small RNA and degr
215  novo ChIP-seq peak prediction and is useful for inferring TF-binding peaks in new experimental condi
216         Our results provide a physical basis for inferring that greenhouse warming is likely to contr
217 any particular season is an unreliable basis for inferring that the year-round average kill rate woul
218      We describe a machine-learning approach for inferring the activity levels of all unexplored sing
219     Here we present RNA timestamps, a method for inferring the age of individual RNAs in RNA-seq data
220 lele age estimates to power a rapid approach for inferring the ancestry shared between individual gen
221   We present SVclone, a computational method for inferring the cancer cell fraction of structural var
222  have taken advantage of a combined approach for inferring the causes of range limits.
223 ak repair (HDR) functional assay as a method for inferring the clinical relevance of VUS in the DBD o
224 the multiple sequence alignment of a protein for inferring the co-evolutionary sectors.
225 oPlotter, an unbiased segmentation algorithm for inferring the compositional organization of genomes.
226 dentifying ancestry components correctly and for inferring the correct tree.
227 ns and apes may provide valuable information for inferring the demographic history of these species,
228        Recently, methods have been developed for inferring the DFE that use information from the alle
229 informed choice of outgroup species suitable for inferring the directions of changes, including testi
230 an pre-implantation development is essential for inferring the earliest cell fate decisions.
231 . sinense genome provides a unique reference for inferring the early evolution of eudicots and the me
232 90, Jotun Hein proposed using this criterion for inferring the evolution of sequences subject to reco
233 with diverse evolutionary models, a pipeline for inferring the evolutionary history of a gene family
234  algorithms, we built an integrated pipeline for inferring the evolutionary history of a given gene f
235 tionary alignment modeler, called "Ortheus," for inferring the evolutionary history of a multiple ali
236                       An important objective for inferring the evolutionary history of gene families
237            Here, we propose Canopy, a method for inferring the evolutionary phylogeny of a tumor usin
238                       We develop an approach for inferring the fractional fire contribution to ambien
239 ac Ca2+ release process and a general method for inferring the functional properties of transmembrane
240 (PANTHER) is a comprehensive software system for inferring the functions of genes based on their evol
241 a an unsupervised machine learning algorithm for inferring the gene targets of sets of TF binding sit
242 easonal migration has long posed a challenge for inferring the geographic origins of migratory specie
243 , and uses less memory than existing methods for inferring the human genome at high resolution (10 kb
244                     We also develop a method for inferring the largest common sub-paths within each o
245 t the value of using modern humans as models for inferring the limits of hominin arboreality.
246                          We present a method for inferring the mechanism most accurately capturing a
247 overcome this problem with a novel framework for inferring the metabolic functions of a cell before m
248 mptions leads to similar solution strategies for inferring the model parameters in both variable type
249  robust, efficient, assumption-free approach for inferring the molecular mechanisms that underlie the
250 al areas, it also has important implications for inferring the nature and epidemiological consequence
251 ter estimation and model selection technique for inferring the number and configuration of promoter s
252                                              For inferring the number of individual gene loss or gain
253 ian model comparison then provides machinery for inferring the optimal order over the group of subjec
254                Here, we discuss two criteria for inferring the optimal tree topology from data sets w
255                     We then propose a method for inferring the order of fate decisions.
256 s is an essential tool of classical genetics for inferring the order of function of genes in a common
257 ation, we have developed an automatic method for inferring the origins of DBD families and their spec
258 his paper is to develop efficient algorithms for inferring the parameters of a general class of Gauss
259                 PopABC is a computer package for inferring the pattern of demographic divergence of c
260 t a method called 'genomic neighbour typing' for inferring the phenotype of a bacterial sample by ide
261 logy-based phylogeny for the genus Gallotia, for inferring the phylogenetic position of extinct speci
262                 We present a Bayesian method for inferring the phylogenetic relationship among relate
263 le to the number of synonymous substitutions for inferring the phylogenetic tree in the SG method, an
264  characters of each type that have been used for inferring the phylogeny of mammals, we find that on
265  this new tool is fast in speed and accurate for inferring the phylogeny of organisms.
266  for identifying the optimal feature lengths for inferring the phylogeny of prokaryotes, strictly spe
267 rate an ST, which results in a powerful tool for inferring the population structure of this pathogen,
268  studies mapping genotypes to phenotypes and for inferring the power of natural selection in human hi
269  with respect to alternative parsimony rules for inferring the presence of precursor architectures in
270 new, to our knowledge, method developed here for inferring the principal curves.
271 e Gibbs sampler is described, and procedures for inferring the probability of yet to be observed futu
272 sts, we also developed an in silico approach for inferring the relative impact of a mutation on RC ba
273                       We report a new method for inferring the scaled mutation rate, theta = 2Neu, an
274  promising two-dimensional chemical strategy for inferring the secondary and tertiary structures that
275                      We present a new method for inferring the SFS using one or two outgroups that at
276 ly, I use the distance-based Bayesian method for inferring the single most likely ancestral codon fro
277 flexible and computationally feasible method for inferring the sources of aneuploidy is thus crucial.
278    Here, we developed and validated a method for inferring the spatial organization of sequential bio
279 icle we present a novel computational method for inferring the strain tree despite massive gene tree
280 gnitude over the methods reported previously for inferring the structure of dynamic networks, such as
281 ases and provides a widely applicable method for inferring the underlying helicase kinetics from forc
282 mporal dynamics of brain activity is crucial for inferring the underlying synaptic and nonsynaptic me
283 d indicate that OFC is specifically required for inferring the value of expected outcomes.
284    This is evidence that the VMF is critical for inferring the value of whole objects in a multiattri
285                              Several methods for inferring this parameter have been proposed, with di
286                         Mathematical methods for inferring time to extinction have been widely applie
287                    We propose a novel method for inferring transcriptional regulation using a simple,
288                    Here, we develop a method for inferring translation elongation kinetics from ribos
289 egration of genomic and epidemiological data for inferring transmission chains.
290 (VNTR)-based clustering, it was insufficient for inferring transmission in the majority of cases.
291  study, we test previously described methods for inferring transmission stage investment against simu
292  direct transmission inference (DTI) problem for inferring transmission trees that support multi-stra
293   This work highlights a powerful technology for inferring transport function and quantifying nutrien
294 e.g., road kill) should be used with caution for inferring trophic ecology as decay can result in sig
295  implemented in publicly available software, for inferring tumor phylogenies on data from potentially
296         This argues that the VMF is critical for inferring value from configural information to guide
297  The orbitofrontal cortex (OFC) is necessary for inferring value in tests of model-based reasoning, i
298 ation for examining the accuracy of NJ trees for inferring very large phylogenies.
299            Here, we set out a novel approach for inferring viral transmission bottlenecks; our method
300 veloping statistical and computational tools for inferring 'who infected whom' in an infectious disea

 
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