SNPlice: variants that modulate Intron retention from RNA-sequencing data.
about
RNA2DNAlign: nucleotide resolution allele asymmetries through quantitative assessment of RNA and DNA paired sequencing dataIntegrated genome and transcriptome sequencing identifies a noncoding mutation in the genome replication factor DONSON as the cause of microcephaly-micromelia syndrome.Alternative splicing complexity contributes to genetic improvement of drought resistance in the rice maintainer HuHan2B.Systematic pan-cancer analysis of somatic allele frequency.
P2860
SNPlice: variants that modulate Intron retention from RNA-sequencing data.
description
2014 nî lūn-bûn
@nan
2014 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
SNPlice: variants that modulate Intron retention from RNA-sequencing data.
@ast
SNPlice: variants that modulate Intron retention from RNA-sequencing data.
@en
type
label
SNPlice: variants that modulate Intron retention from RNA-sequencing data.
@ast
SNPlice: variants that modulate Intron retention from RNA-sequencing data.
@en
prefLabel
SNPlice: variants that modulate Intron retention from RNA-sequencing data.
@ast
SNPlice: variants that modulate Intron retention from RNA-sequencing data.
@en
P2093
P2860
P356
P1433
P1476
SNPlice: variants that modulate Intron retention from RNA-sequencing data.
@en
P2093
Anelia Horvath
Maria Kokkinaki
Mercedeh Movassagh
Nady Golestaneh
Nathan J Edwards
Prakriti Mudvari
P2860
P304
P356
10.1093/BIOINFORMATICS/BTU804
P407
P577
2014-12-06T00:00:00Z