SMaSH: a benchmarking toolkit for human genome variant calling.
about
Transposable element detection from whole genome sequence dataBest practices for evaluating single nucleotide variant calling methods for microbial genomicsReview of current methods, applications, and data management for the bioinformatics analysis of whole exome sequencing.RDDpred: a condition-specific RNA-editing prediction model from RNA-seq data.In-depth comparison of somatic point mutation callers based on different tumor next-generation sequencing depth dataDetailed comparison of two popular variant calling packages for exome and targeted exon studiesAn analytical framework for optimizing variant discovery from personal genomes.VarSim: a high-fidelity simulation and validation framework for high-throughput genome sequencing with cancer applications.A call for benchmarking transposable element annotation methods.SNVSniffer: an integrated caller for germline and somatic single-nucleotide and indel mutations.Toward better understanding of artifacts in variant calling from high-coverage samples.An Evaluation Framework for Lossy Compression of Genome Sequencing Quality Values.Jointly aligning a group of DNA reads improves accuracy of identifying large deletions.ToTem: a tool for variant calling pipeline optimization.geck: trio-based comparative benchmarking of variant calls
P2860
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P2860
SMaSH: a benchmarking toolkit for human genome variant calling.
description
2014 nî lūn-bûn
@nan
2014 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի հունիսին 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
SMaSH: a benchmarking toolkit for human genome variant calling.
@ast
SMaSH: a benchmarking toolkit for human genome variant calling.
@en
type
label
SMaSH: a benchmarking toolkit for human genome variant calling.
@ast
SMaSH: a benchmarking toolkit for human genome variant calling.
@en
prefLabel
SMaSH: a benchmarking toolkit for human genome variant calling.
@ast
SMaSH: a benchmarking toolkit for human genome variant calling.
@en
P2093
P2860
P356
P1433
P1476
SMaSH: a benchmarking toolkit for human genome variant calling.
@en
P2093
Ameet Talwalkar
Christopher Hartl
David Patterson
Jesse Liptrap
Jonathan Terhorst
Julie Newcomb
Kristal Curtis
Ma'ayan Bresler
Yun S Song
P2860
P304
P356
10.1093/BIOINFORMATICS/BTU345
P407
P577
2014-06-03T00:00:00Z