1 Sequencing of 1,314 SARS-CoV-2 viral genomes from availa
2 red with deep whole-genome and transcriptome
sequencing of 100 castration-resistant prostate metastas
3 Through RNA-
sequencing of 100,987 individual cells from 7 primary, 2
4 Longitudinal
sequencing of 12 patients with 2-5 serial plasma samples
5 gression, we performed ultrahigh depth exome
sequencing of 124 DNA damage repair/response (repairome)
6 Through whole-genome
sequencing of 13 melanoma metastases sampled at autopsy
7 Whole-exome
sequencing of 159 prospectively resected pituitary adeno
8 8 million variants derived from whole genome
sequencing of 160 islet autoantibody positive subjects,
9 n pathogenic E. coli, we carried out genomic
sequencing of 162 isolates obtained from patient blood c
10 dance of Staphylococcus were assessed by DNA
sequencing of 16S ribosomal RNA, and absolute S. aureus
11 Sequencing of 16S rRNA gene amplicons from microbiomes h
12 opulations and single cells were analysed by
sequencing of 16S rRNA genes in the oligotrophic North P
13 Here we performed bulk RNA
sequencing of 17 organs and plasma proteomics at 10 ages
14 omosome-scale reference assembly and deep re-
sequencing of 183 cultivated and wild Digitaria accessio
15 tions in NTRK2 and NTRK3 identified via deep
sequencing of 185 patients with hematological malignanci
16 Sequencing of 186 other nonfamilial cases identified ano
17 etic variants were identified by whole-exome
sequencing of 2 patients with familial IMD.
18 Here, we performed deep RNA
sequencing of 200 Drosophila Genetic Reference Panel inb
19 its mutational profile, we conduct targeted
sequencing of 205 genes for 2,105 CRC cases with surviva
20 We performed targeted ultra-deep
sequencing of 25 genes and Digital Droplet PCR of TERT p
21 We performed whole-exome
sequencing of 250 parent-offspring trios, and observed e
22 In this study, we performed whole exome
sequencing of 264 individuals from 63 multiplex families
23 Sanger
sequencing of 30 additional formalin-fixed metastases en
24 le-cell RNA and paired T cell receptor (TCR)
sequencing of 30,604 T cells from 7 patients.
25 opathic NOA and SO, we performed whole-exome
sequencing of 314 unrelated patients of Chinese Han orig
26 both health and disease using 16S rRNA gene
sequencing of 410 individuals from across the world.
27 Single-cell
sequencing of 42,000 tumor cells revealed widespread het
28 Sequencing of 427 new genomes and analysis of a geograph
29 CNVs were generated from exome
sequencing of 4913 schizophrenia cases and 6188 control
30 Here we combine single-cell RNA
sequencing of 51,199 mouse cells of ectodermal origin, g
31 We also performed whole-exome
sequencing of 54 liver nodules from patients with cirrho
32 Single-cell
sequencing of 547 individual cancer cells from eight sol
33 Sequencing of 57 sCJD patients, and healthy controls rev
34 Therefore, whole-genome
sequencing of 756 child-parent trios of European, Colomb
35 Shallow whole-genome
sequencing of 777 biopsies, sampled from 88 patients in
36 enome, exome, transcriptome, and methylation
sequencing of 83 canine gliomas, we found alterations sh
37 g on palms, soles or nail beds, whole genome
sequencing of 87 tumors with matching transcriptome sequ
38 RNA-
sequencing of 90 resected specimens and unsupervised cla
39 Sequencing of a bacterial artificial chromosome in the f
40 allocate the limited sequencing budget: deep
sequencing of a few cells or shallow sequencing of many
41 ndidates, based on whole-genome and iPSC RNA
sequencing of a HLHS family-trio.
42 We performed whole-exome
sequencing of a hundred trios (probands and their parent
43 forms of MNG likely exist.METHODSWhole-exome
sequencing of a kindred with early-onset MNG and schwann
44 ted in vivo by chromatin immunoprecipitation
sequencing of a patient-derived xenograft.
45 Through the use of GWAS and subsequent
sequencing of a PRA case, we have identified a LINE-1 in
46 y using V4 and full-length 16S ribosomal RNA
sequencing of a series of fecal samples, we found that g
47 tribute to brain metastases and that genomic
sequencing of a sufficient number of metastatic tumors c
48 Genome
sequencing of actinomycetes reveals an untapped reservoi
49 Single cell RNA-
sequencing of activated B cells and construction of diff
50 The
sequencing of ADT with prostate-directed RT has signific
51 We conducted a comprehensive single-cell RNA
sequencing of advanced human carotid endarterectomy samp
52 We conducted whole-genome
sequencing of all 1,575 available GAS macrolide-resistan
53 lidated PCR assays followed by bidirectional
sequencing of amplicons) was performed on all samples as
54 a lack of clarity regarding the influence of
sequencing of androgen deprivation therapy (ADT) and rad
55 ing droplet- and plate-based single-cell RNA
sequencing of approximately 75,000 human cells across al
56 replication, we performed follow-up targeted
sequencing of ASH1L in additional 524 unrelated TS sampl
57 Sequencing of automatically prepared libraries from T-ce
58 RNA-
sequencing of axillary nodes from StMSI1-OE and StBMI1-1
59 Next generation
sequencing of B cell receptor (BCR) repertoires offers a
60 utant ZFP36L1 as well as whole transcriptome
sequencing of bladder cancer cells {plus minus} tet-on Z
61 Sequencing of bladder cancer has revealed that loss-of-f
62 le factors on CH, we performed deep targeted
sequencing of blood DNA from 52 monozygotic (MZ) and 27
63 eoclast ablation by denosumab (DMAb) and RNA-
sequencing of bone biopsies from postmenopausal women to
64 High-throughput genome
sequencing of both isolates and metagenomic samples comb
65 Single-cell RNA
sequencing of both organoids and primary tissue identifi
66 ed dragon (Pogona vitticeps) using small RNA
sequencing of brain, heart, and skeletal muscle from ind
67 ng these karyotypes from high-throughput DNA
sequencing of bulk tumor samples is complicated because
68 se findings highlight the need for long-read
sequencing of cancer genomes for the precise analysis of
69 ole-genome sequencing profiles from bulk DNA
sequencing of cancer tissues is fueling the application
70 -exome sequencing and whole-genome bisulfite
sequencing of cell free DNA (cfDNA) and of matched metas
71 Sequencing of cell-sorted fractions reveals members of t
72 Global run-on
sequencing of cells overexpressing PAX2, when coupled wi
73 Sequencing of cfDNA from seven plasma samples from trans
74 Our study supports
sequencing of CFH, CFI, and C3 genes because they harbor
75 By genome
sequencing of CHO-MG cells, we identified mutations in a
76 Single-molecule long-read
sequencing of chromatin stencils enabled nucleotide-reso
77 Deeper and broader
sequencing of circulating tumor DNA (ctDNA) has identifi
78 Here we used whole-genome
sequencing of clonal cell isolates that developed chemot
79 Whole-genome
sequencing of clonal organoids before and after this exp
80 performed a gene expression study using RNA
sequencing of CNON cells from 111 control subjects and 1
81 Metagenomics is the collective DNA
sequencing of coexisting microbial organisms in an envir
82 Lynch syndrome patients using 16S rRNA gene
sequencing of colon biopsies, coupled with metagenomic a
83 of tools for neoepitope prediction from DNA
sequencing of complementary tumor and normal patient sam
84 Here we have performed whole genome
sequencing of consecutive M. tuberculosis isolates obtai
85 RNA-
sequencing of DAC-treated tumors revealed increased expr
86 nscript abundances were determined using RNA
sequencing of developing wood tissues from upright trees
87 Although
sequencing of DIDS-resistant HCMV revealed enrichment of
88 Single-cell or single-nuclei mRNA
sequencing of dissociated mouse kidneys and of dissected
89 encing (lrTAPS) for targeted base-resolution
sequencing of DNA methylation and hydroxymethylation in
90 yping assays and high-throughput genome-wide
sequencing of DNA translocations, this is achieved while
91 Whole-exome
sequencing of donor and recipient DNA and single-cell RN
92 expression associated with CUD by using RNA
sequencing of dorsal-lateral prefrontal cortex neurons.
93 We performed proteomic
sequencing of dorsolateral prefrontal cortex in 438 olde
94 mRNA
sequencing of E18 cortex revealed 320 differentially exp
95 Here we used multilocus amplicon
sequencing of eDNA to survey biodiversity from an eighte
96 Single-cell RNA-
sequencing of eight post-treatment samples demonstrates
97 Single-cell RNA
sequencing of embryos can resolve the transcriptional la
98 Sequencing of endogenous organic molecules in fossil inv
99 RNA-
sequencing of engrafted hESC-CMs confirmed the increased
100 The data from DNA and RNA
sequencing of epidermis and SCCIS provide insights regar
101 With this method, we performed small RNA
sequencing of exosomes (EXOs), microvesicles (MVs) and s
102 n the langur genus Presbytis through shotgun
sequencing of faecal DNA (P. femoralis femoralis, P. f.
103 ature survey and empirical study how shotgun
sequencing of faecal DNA is a still underutilized but po
104 pecific internal transcribed spacer amplicon
sequencing of fecal samples.
105 pled with metagenomic and metatranscriptomic
sequencing of feces.
106 Single-cell RNA
sequencing of five TNBCs revealed two cancer-associated
107 low determines optimal samples for effective
sequencing of fossil coral proteins, allowing comparison
108 RNA
sequencing of freshly isolated CTCs from breast cancer p
109 roplet PCR, single-genome amplification, and
sequencing of full-length (FL) envelope HIV.
110 at electrodes were studied using the PacBio
sequencing of full-length 16S rRNA gene.
111 We report nanopore
sequencing of full-length cDNA from CLL samples with and
112 The
sequencing of G. margarita genome reveals the importance
113 , emphasis should be placed in targeted gene
sequencing of genes known to cause adRP, such as RHO and
114 Here, we performed RNA
sequencing of genetically labeled MrgprA3(+) neurons und
115 As genome skimming (low-pass
sequencing of genomes at low coverage, precluding assemb
116 Sequencing of genomes of passaged and cloned viruses rev
117 We further used 16S rRNA gene amplicon
sequencing of genomic DNA (gDNA) and complementary DNA (
118 triction fragments (TRFs), along with MinION
sequencing of genomic DNA allowed us to document the pre
119 Targeted
sequencing of genomic regions is a cost- and time-effici
120 Functional assays, as well as direct
sequencing of genomic sgRNA target sites, indicates that
121 Next-generation
sequencing of germline DNA in 2,160 early-onset breast c
122 We have carried out next-generation
sequencing of glandular trichomes of N. tabcaum and inve
123 Extensive genomic
sequencing of gliomas, different cell types, brain tissu
124 nts (n = 153) using targeted high-throughput
sequencing of &
gt;300 potential candidate genes.
125 Sequencing of gut transcripts revealed PE-fed larvae ret
126 the mass spectrometry-based toolkit for the
sequencing of heparan sulfate and structurally related b
127 At the molecular level, RNA
sequencing of HF cardiac fibroblasts highlighted the ove
128 mRNA
sequencing of hippocampal subregions indicated DEGs in t
129 Next-generation targeted
sequencing of HLA-DQA1 and -DQB1 in Swedish newly diagno
130 he profiling of bacterial communities by the
sequencing of housekeeping genes such as that encoding t
131 We performed single-cell RNA
sequencing of human eyelid skin from healthy individuals
132 d electron microscopy, while single-cell RNA
sequencing of human kidneys showed expression of the cog
133 Single-cell RNA-
sequencing of human lungs, including those from idiopath
134 we performed UV cross-linking, ligation and
sequencing of hybrids (CLASH) to uncover Hfq-associated
135 Through intensive surveillance and genetic
sequencing of IAVs in exhibition swine in six U.S. state
136 multicolour 'Brainbow' cell-fate mapping and
sequencing of immunoglobulin genes from single cells, we
137 mor's evolutionary trajectory requires dense
sequencing of individual clones or single cells.
138 controlled trial of rapid diagnostic genomic
sequencing of infants in regional ICUs.
139 Exome
sequencing of infertile males revealed three heterozygou
140 Single-cell RNA-
sequencing of injured sciatic nerve identifies five macr
141 e glycans, yet current methods do not afford
sequencing of intact glycopeptides.
142 Top-down
sequencing of intact proteins and multiprotein complexes
143 RNA
sequencing of isolated bronchi confirmed the IL-13-media
144 ta from known reference strains and Illumina
sequencing of isolates cultured from the same patients.
145 We used UNCALLED to deplete
sequencing of known bacterial genomes within a metagenom
146 Total RNA
sequencing of liver biopsy specimens from the obese stea
147 In summary, direct-from-sample
sequencing of M. tuberculosis genomes was facilitated by
148 t: deep sequencing of a few cells or shallow
sequencing of many cells?
149 Since whole-genome
sequencing of many crops has been achieved, crop functio
150 RNA-
sequencing of MBC subsets from multiple tissues revealed
151 Bulk and single-cell-targeted
sequencing of MDS recurrently mutated genes in CD34+ pro
152 dioactive and stable isotopes of carbon, RNA
sequencing of metabolically important enzymes, and immun
153 um, followed by immunoaffinity isolation and
sequencing of MHC class I- and II-bound peptides.
154 Shotgun
sequencing of microbial communities, referred to initial
155 Here, we applied whole-genome shotgun
sequencing of microbial DNA extracted directly from the
156 rofiles of 4 tissue types were compared, and
sequencing of miRNA, pre-miRNA, and mRNA was performed i
157 Extraction and high-throughput
sequencing of miRNAs were performed using samples collec
158 Next-generation
sequencing of mitochondrial DNA (mtDNA) was performed fo
159 ding, biocytin staining, and single-cell RNA
sequencing of more than 1,300 neurons in adult mouse pri
160 RNA
sequencing of morphologically distinct macrophages ident
161 nalyzed data from a study of single-cell RNA
sequencing of mouse cortical neurons.
162 Using nuclear RNA
sequencing of mouse enteric neurons that represent disti
163 Sequencing of mtDNA identified a mutation in the mitocho
164 an be studied genome wide by high-throughput
sequencing of nascent and newly synthesized RNA.
165 Sequencing of nascent RNA to explore DMD transcription d
166 Here, using next-generation
sequencing of near-full-length single HIV-1 genomes and
167 ing single-cell RNA-sequencing with bulk RNA-
sequencing of Nkx2-1 mutants and NKX2-1 ChIP-sequencing
168 Therefore, through transcriptome
sequencing of normal, primary, and distant mCRC tissues
169 Next-generation
sequencing of NP396-specific TCRs showed that exhaustion
170 Genome
sequencing of NRRL 8095 identified the acrophiarin gene
171 We performed nanopore
sequencing of nucleosome occupancy and methylome (nanoNO
172 ANCE Here, we report the discovery, via deep
sequencing, of numerous noncoding RNAs (ncRNAs) derived
173 h the development of the high-throughput DNA
sequencing of organisms at the population level, an appl
174 In this report, we present single-cell RNA
sequencing of over 38,000 cells from mouse digit tip bla
175 cing (RenSeq) with single-molecule real-time
sequencing of PacBio for 18 accessions in Solanaceae, in
176 Whole genome
sequencing of paired isolates was used to identify mecha
177 Targeted cloning, mapping, and
sequencing of parental and novel telomeric restriction f
178 Here, we use single cell RNA-
sequencing of patient tumors to identify three prognosti
179 However, the conventional Sanger
sequencing of PCR products for the authentication of sea
180 brain in utero, followed by single-cell RNA-
sequencing of perturbed cells in the postnatal brain.
181 Illumina GAIIx
sequencing of plants collected during end of vegetative
182 Single-cell RNA-
sequencing of plaque immune cells revealed that unlike T
183 cell culture for the detection and real-time
sequencing of polioviruses in stool and environmental sa
184 Whole-exome
sequencing of post-mortem plasma-derived cell-free DNA a
185 We performed targeted
sequencing of pre-treatment and PD tumor samples from 54
186 n this study, next-generation virome capture
sequencing of primary and metastatic tumors were perform
187 ts who underwent targeted massively parallel
sequencing of primary ECs between 2014 and 2018 and preo
188 Next generation
sequencing of primary RMS tumors identified a single nuc
189 So far,
sequencing of protein N- and C-termini has been limited
190 concept that readily enables unbiased ladder
sequencing of protein N- and C-termini.
191 DNA
sequencing of purified products yielded Phred quality sc
192 genetic factors that influence WT risk, with
sequencing of rare familial cases and large WT cohorts r
193 The Illumina MiSeq 16S rRNA gene amplicon
sequencing of reactors showed that the microbial communi
194 results were analyzed by bi-directional PCR/
sequencing of residual blood culture samples.
195 a combination of in vivo testing and direct
sequencing of resistance genes folP1, rpoB, and gyrA.
196 Using single-cell RNA
sequencing of retinal cells isolated from C57BL/6J mice,
197 microbiota, we performed 16S rRNA gene-based
sequencing of retrospective tumor and matched normal tis
198 Using antibody-independent ChIP-
sequencing of REVERBalpha in mouse liver, we reveal a hi
199 rcling the genome more than once, and Sanger
sequencing of reverse transcription-PCR (RT-PCR) product
200 Deep
sequencing of ribosomal DNA (rDNA) suggests thousands of
201 ciated with repetitive behavior by using RNA
sequencing of ribosome-associated mRNA.
202 High-throughput
sequencing of RNA (RNA-seq) has expedited the exploratio
203 xt-generation sequencing (mNGS), the shotgun
sequencing of RNA and DNA from clinical samples, has pro
204 Here, by performing deep single-cell
sequencing of RNA and T cell receptors in patients with
205 Sequencing of RNA from the endothelial cells uncovered t
206 vel transcriptome using single-cell RNA-seq (
sequencing of RNA reverse transcribed into cDNA) and fou
207 diversity was examined using high-throughput
sequencing of rpoB amplicons generated with a Streptomyc
208 OM and PLG, exome and Sanger sequencing, RNA-
sequencing of saliva and middle ear samples, 16S rRNA se
209 Recently,
sequencing of salivary-gland mRNA libraries revealed inc
210 Using whole-exome
sequencing of samples from 20 PCa families, with three o
211 SWGA enables the successful whole genome
sequencing of samples with low parasite density (i.e. on
212 Genome
sequencing of SARS-CoV-2 allows the reconstruction of it
213 Whole genome
sequencing of select transformants demonstrated that rec
214 otion of a single transition region and then
sequencing of several such moving transition regions to
215 gene (rRNA) polymerase chain reaction (PCR)/
sequencing of SF and compare it with that of SF culture.
216 ituents of the whole retinal layers, and the
sequencing of shortwave length sensitive opsin 1 (SWS1)
217 Exome
sequencing of siblings with severe neurodevelopmental de
218 16S rRNA gene
sequencing of SIgA-coated/uncoated bacteria (IgA-Biome)
219 orkflow to perform targeted and whole-genome
sequencing of small populations of cells (typically 100-
220 Moreover,
sequencing of small RNA molecules enabled the identifica
221 By deep
sequencing of small RNAs from Bactrocera dorsalis early
222 chain reaction-detected parasites using deep
sequencing of SP-resistance alleles.
223 However, genome
sequencing of specimens is challenging because of low ba
224 isease.Methods: We performed single-cell RNA
sequencing of sputum cells from nine subjects with CF an
225 the relative abundance identified in direct
sequencing of sputum samples; importantly, culture enric
226 and identify, through PCR amplification and
sequencing of the 16S-rRNA gene, the potential presence
227 Most interestingly, RNA
sequencing of the 3 subsets revealed that G-MDSC-related
228 Single-cell RNA
sequencing of the adult pituitary reveals similar compet
229 Full genome
sequencing of the ANDV strain involved in this outbreak
230 ges at electromyography, we recommend direct
sequencing of the ATP2A1 gene or next generation sequenc
231 ongoing controversies regarding the optimal
sequencing of the available and expanding treatment opti
232 ect study sites, and we used high-throughput
sequencing of the bacterial 16S rRNA gene to assess whet
233 or Schistosoma mansoni, using Illumina MiSeq
sequencing of the bacterial 16S V4 rDNA.
234 d by high-coverage, ultra-long-read nanopore
sequencing of the complete hydatidiform mole CHM13 genom
235 Recent genome
sequencing of the constitutive model CAM species Kalanch
236 otor methylation was quantified using Sanger
sequencing of the CpG sites 74-98 within the MGMT promot
237 RNA
sequencing of the forebrain cortex indicated a potential
238 on of PC intake, together with 16S rRNA gene
sequencing of the gut microbiota, and faecal and plasma
239 RNA
sequencing of the highly motile cells revealed different
240 RNA-
sequencing of the hippocampus revealed that stress incre
241 Deep
sequencing of the HIV DNA partial env gene was performed
242 Further, scRNA
sequencing of the HO site after injury with or without i
243 Since the
sequencing of the human mitochondrial genome and the dis
244 Single-cell
sequencing of the human TM revealed similar cell types a
245 Single-cell RNA
sequencing of the immune compartment showed that IL8 is
246 After injury, single-cell (sc) RNA
sequencing of the injury site reveals an early increase
247 Nucleotide
sequencing of the inserted DNA confirmed it was introduc
248 the C. auris resistance profile, and Sanger
sequencing of the internal transcribed spacer (ITS) and
249 conventional crop management using Illumina
sequencing of the internal transcribed spacer (ITS) gene
250 Additionally, the recent
sequencing of the Ixodes scapularis genome and character
251 =10(4) CFU/ml of N. gonorrhoeae was present,
sequencing of the large majority of the genome was frequ
252 rmed a genetic screen from deep whole genome
sequencing of the large NIMH family-based Alzheimer's Di
253 Single-cell RNA-
sequencing of the microglial chimeric mouse brains revea
254 dentification of vertebrate tissue relies on
sequencing of the mitochondrial cytochrome oxidase I (CO
255 RNA
sequencing of the mutant line identified 2220 differenti
256 omes of sheep, with a focus on isolation and
sequencing of the ovine Y chromosome.
257 Viral genome
sequencing of the paired first-positive and reinfection
258 Rapid clinical whole-exome
sequencing of the patients and segregation in available
259 demonstrate that affinity selection and deep
sequencing of the phage library provide sufficient resol
260 MIC, pDST and whole genome
sequencing of the pncA, rpsA and panD genes were used to
261 At its inception, before the
sequencing of the rat genome, RGD started with only a fe
262 After
sequencing of the remaining intact strands, this allows
263 Deep
sequencing of the repertoire of antigen receptor-encodin
264 Here we used amplicon
sequencing of the ribosomal RNA internal transcribed spa
265 genome sequencing data with single-cell mRNA
sequencing of the same inbred fly strain to map transpos
266 The read counts that result from RNA
sequencing of the samples extracted from the same experi
267 We performed whole-genome
sequencing of the SKBR3 breast cancer cell line and pati
268 Deep
sequencing of the SLC26A9 gene in 762 individuals with C
269 Targeted
sequencing of the stem cell product from 629 MM patients
270 Targetted re-
sequencing of the Sub1A, Sub1B and Sub1C genes identfied
271 rack individual T cell clones through paired
sequencing of the T cell receptor genes and high-dimensi
272 Single-cell RNA
sequencing of the third instar larval brain shows that p
273 Primer ID deep
sequencing of the V1/V3 region of the HIV-1 env gene was
274 Deep
sequencing of the viral episomes and host chromosomes in
275 how genomics extends beyond consensus-level
sequencing of the virus to include intra-host viral tran
276 genesis, we have carried out single cell RNA
sequencing of the zebrafish hindbrain at three different
277 Whole-exome
sequencing of these cells after defined numbers of popul
278 explained the high-risk family segregation;
sequencing of these regions will be needed to discover s
279 The optimal
sequencing of these therapies is unclear.
280 t-generation sequencing technologies allowed
sequencing of thousands of genomes.
281 le-cell barcoding technologies enable genome
sequencing of thousands of individual cells in parallel,
282 Whole transcriptome RNA-
Sequencing of tumors from 23 patients with MPBC-HGT1 and
283 arative epigenomic profiling and single-cell
sequencing of two related teleost fish uncovered species
284 Metagenomic techniques have enabled genome
sequencing of unknown viruses without isolation in cell
285 with seven antibiotics and for whole-genome
sequencing of up to 5,000 isolates.
286 We have previously shown metagenomic
sequencing of urine samples from men with urethral gonor
287 Using Nanopore
sequencing of urine samples from men with urethral gonor
288 Shotgun
sequencing of vaginal swabs from postmenopausal women se
289 Single-cell RNA
sequencing of vascular and glial cells revealed that apo
290 Single-cell RNA
sequencing of vascular cells in mice suggested that the
291 es in another 39 patients by high-throughput
sequencing of vector-integration sites.
292 Deep
sequencing of viral samples illuminated the within-host
293 We performed shotgun metagenomic
sequencing of virus-like particles.
294 we performed T cell receptor beta (TCRbeta)
sequencing of virus-specific CD8 T cells during chronic
295 Through subgenomic
sequencing of viruses present in residual plasma from an
296 High-throughput short-read and long-read
sequencing of VLP DNA (VLP DNA-seq) revealed a comprehen
297 next-generation sequencing, have enabled the
sequencing of whole ancient genomes.
298 RNA
sequencing of whole lung identified 33 FSTL-1-regulated
299 RNA
sequencing of wild-type and FSTL-1 Hypo mice identified
300 Using whole-genome
sequencing of zebrafish mutants isolated in an unbiased