SNVSniffer: an integrated caller for germline and somatic single-nucleotide and indel mutations.
about
Detecting very low allele fraction variants using targeted DNA sequencing and a novel molecular barcode-aware variant callerISOWN: accurate somatic mutation identification in the absence of normal tissue controls.Comprehensive benchmarking of SNV callers for highly admixed tumor data.Analysis and Annotation of Whole-Genome or Whole-Exome Sequencing Derived Variants for Clinical Diagnosis.A review of somatic single nucleotide variant calling algorithms for next-generation sequencing data.
P2860
SNVSniffer: an integrated caller for germline and somatic single-nucleotide and indel mutations.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
SNVSniffer: an integrated call ...... ucleotide and indel mutations.
@ast
SNVSniffer: an integrated call ...... ucleotide and indel mutations.
@en
type
label
SNVSniffer: an integrated call ...... ucleotide and indel mutations.
@ast
SNVSniffer: an integrated call ...... ucleotide and indel mutations.
@en
prefLabel
SNVSniffer: an integrated call ...... ucleotide and indel mutations.
@ast
SNVSniffer: an integrated call ...... ucleotide and indel mutations.
@en
P2093
P2860
P1433
P1476
SNVSniffer: an integrated call ...... ucleotide and indel mutations.
@en
P2093
Bertil Schmidt
Martin Loewer
Yongchao Liu
P2860
P2888
P356
10.1186/S12918-016-0300-5
P478
10 Suppl 2
P577
2016-08-01T00:00:00Z
P6179
1018494029