Identification of rare germline copy number variations over-represented in five human cancer types.
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ExCNVSS: A Noise-Robust Method for Copy Number Variation Detection in Whole Exome Sequencing Data.Genome-wide copy number variation (CNV) detection in Nelore cattle reveals highly frequent variants in genome regions harboring QTLs affecting production traits.QuaDMutEx: quadratic driver mutation explorerLong noncoding RNA CNALPTC1 promotes cell proliferation and migration of papillary thyroid cancer via sponging miR-30 family.
P2860
Identification of rare germline copy number variations over-represented in five human cancer types.
description
2015 nî lūn-bûn
@nan
2015 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
name
Identification of rare germlin ...... ed in five human cancer types.
@ast
Identification of rare germlin ...... ed in five human cancer types.
@en
type
label
Identification of rare germlin ...... ed in five human cancer types.
@ast
Identification of rare germlin ...... ed in five human cancer types.
@en
prefLabel
Identification of rare germlin ...... ed in five human cancer types.
@ast
Identification of rare germlin ...... ed in five human cancer types.
@en
P2093
P2860
P1433
P1476
Identification of rare germlin ...... ed in five human cancer types.
@en
P2093
Peter J Park
Richard W Park
Simon Kasif
Tae-Min Kim
P2860
P2888
P356
10.1186/S12943-015-0292-6
P577
2015-02-03T00:00:00Z
P5875
P6179
1031366628