A streamlined method for detecting structural variants in cancer genomes by short read paired-end sequencing
about
Quantifying on- and off-target genome editingCharacterization of human chromosomal material exchange with regard to the chromosome translocations using next-generation sequencing dataRAG2 mutants alter DSB repair pathway choice in vivo and illuminate the nature of 'alternative NHEJ'.Sequencing depth and coverage: key considerations in genomic analyses.Role of non-coding sequence variants in cancer.Multidimensional Genome-wide Analyses Show Accurate FVIII Integration by ZFN in Primary Human CellsOff-Target V(D)J Recombination Drives Lymphomagenesis and Is Escalated by Loss of the Rag2 C Terminus.V(D)J Recombination: Mechanism, Errors, and Fidelity.Analysis and annotation of whole-genome or whole-exome sequencing-derived variants for clinical diagnosis.Analysis and Annotation of Whole-Genome or Whole-Exome Sequencing Derived Variants for Clinical Diagnosis.
P2860
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P2860
A streamlined method for detecting structural variants in cancer genomes by short read paired-end sequencing
description
2012 nî lūn-bûn
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2012年の論文
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2012年学术文章
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2012年学术文章
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2012年学术文章
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name
A streamlined method for detec ...... ort read paired-end sequencing
@ast
A streamlined method for detec ...... ort read paired-end sequencing
@en
type
label
A streamlined method for detec ...... ort read paired-end sequencing
@ast
A streamlined method for detec ...... ort read paired-end sequencing
@en
prefLabel
A streamlined method for detec ...... ort read paired-end sequencing
@ast
A streamlined method for detec ...... ort read paired-end sequencing
@en
P2093
P2860
P1433
P1476
A streamlined method for detec ...... ort read paired-end sequencing
@en
P2093
Cory R Lindsay
David B Roth
Efstratios Efstathiadis
Martina Mijušković
Stuart M Brown
Zuojian Tang
P2860
P304
P356
10.1371/JOURNAL.PONE.0048314
P407
P577
2012-10-29T00:00:00Z