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1 cific scoring matrix (PSSM), also known as a position weight matrix.
2 user-defined TFBSs given as a consensus or a position weight matrix.
3 variable sequences, were used to establish a position weight matrix and a matrix similarity (MS) scor
4 n, HIGEDA can identify gapped motifs using a position weight matrix and dynamic programming to genera
5 ree (CART) statistical model, which involves position weight matrix and human-mouse sequence similari
6 microarrays to derive a novel SOX4-specific position-weight matrix and determined that SOX4 binding
7 AR template performance based on sequence: a position weight matrix approach with support vector mach
8 cher description of the MEF2 binding site, a position weight matrix, can be reliably constructed and
9 itional supplementary annotation data (e.g., position weight matrix matches, conservation scores, str
10 dentification algorithm, which is based on a position weight matrix model that does not require addit
11 factor (TF) is typically represented using a position weight matrix model, which implicitly assumes t
12 moter strength and function, we used modular position weight matrix models comprised of each promoter
14 hypergeometric-based scoring function and a position-weight matrix optimization routine to identify
15 uch as sparse profile, dinucleotide profile, position weight matrix profile, Markov motif profile and
16 TFBSs are generally recognized by scanning a position weight matrix (PWM) against DNA using one of a
17 ('words') of length k ('k-mers'), as well as position weight matrix (PWM) and graphical sequence logo
18 ('words') of length k ('k-mers'), as well as position weight matrix (PWM) and graphical sequence logo
24 DSMC) motif discovery technique based on the position weight matrix (PWM) model to locate conserved m
25 lly infer the optimal cutoff threshold for a position weight matrix (PWM) of a motif identified from
27 (TF) binding site analysis using a TRANSFAC position weight matrix (PWM) search, 86% of non-specific
29 red target sequence of a TF in the form of a position weight matrix (PWM), DNA accessibility data (in
33 , fdrMotif combines model optimization [e.g. position weight matrix (PWM)] and significance testing a
35 wly identified sites were used to generate a position-weighted matrix (PWM) for EBNA1's DNA-binding s
37 we developed two methods, Kmer-Sum and PWM (Position Weight Matrix) stacking, for full-length bindin
39 on incorporating p53 binding strength into a position weight matrix, we selected 32 SNPs in putative
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