Long insert whole genome sequencing for copy number variant and translocation detection.
about
Rare variant discovery by deep whole-genome sequencing of 1,070 Japanese individualsNon-random DNA fragmentation in next-generation sequencing.Case report: whole exome sequencing of primary cardiac angiosarcoma highlights potential for targeted therapiesClinical Implementation of Integrated Genomic Profiling in Patients with Advanced Cancers.A somatic reference standard for cancer genome sequencing.Evidence Suggesting That Discontinuous Dosing of ALK Kinase Inhibitors May Prolong Control of ALK+ Tumors.Integrated genomic analyses reveal frequent TERT aberrations in acral melanoma.Cat-D: a targeted sequencing method for the simultaneous detection of small DNA mutations and large DNA deletions with flexible boundaries.Somatic inactivating PTPRJ mutations and dysregulated pathways identified in canine malignant melanoma by integrated comparative genomic analysis
P2860
Q28607995-2049BC3B-48B7-4F62-AFEE-3A1F8CA0359DQ30440990-4D5F1B9A-FBA7-4DC6-945D-F1F33FA82F4CQ30834078-041BD2DB-D568-427C-B533-EAA4DDA1B4A6Q33685000-3EC59FBF-B7A5-45A7-BF6F-A6EB04313F17Q35994200-0195E823-B771-498A-96EF-38F1A7E891E4Q38870250-12524FCE-7173-4C4E-85DD-1890C31DCDA4Q41642490-8A2BB088-D24A-4EFA-BA1E-DB73D5ACDBECQ47109745-FBF8C918-629E-4D98-92ED-F3E8146BBFE3Q58762125-46422EA5-D148-4014-BA4C-BAD9BCCCE16B
P2860
Long insert whole genome sequencing for copy number variant and translocation detection.
description
2013 nî lūn-bûn
@nan
2013 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Long insert whole genome sequencing for copy number variant and translocation detection.
@ast
Long insert whole genome sequencing for copy number variant and translocation detection.
@en
type
label
Long insert whole genome sequencing for copy number variant and translocation detection.
@ast
Long insert whole genome sequencing for copy number variant and translocation detection.
@en
prefLabel
Long insert whole genome sequencing for copy number variant and translocation detection.
@ast
Long insert whole genome sequencing for copy number variant and translocation detection.
@en
P2093
P2860
P356
P1476
Long insert whole genome sequencing for copy number variant and translocation detection.
@en
P2093
Ahmet Kurdoglu
Angela Baker
David W Craig
Glen J Weiss
Irene Cherni
Jessica Aldrich
John D Carpten
Lori Phillips
Rebecca Reiman
Waibhav Tembe
P2860
P356
10.1093/NAR/GKT865
P407
P577
2013-09-25T00:00:00Z