Improving somatic variant identification through integration of genome and exome data.

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Improving somatic variant identification through integration of genome and exome data.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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Improving somatic variant identification through integration of genome and exome data.

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Improving somatic variant identification through integration of genome and exome data.

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Improving somatic variant identification through integration of genome and exome data.

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Improving somatic variant identification through integration of genome and exome data.

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Improving somatic variant identification through integration of genome and exome data.

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Improving somatic variant identification through integration of genome and exome data.

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P1476

Improving somatic variant identification through integration of genome and exome data

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P2093

Liqing Zhang

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Siu-Ming Yiu

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Vinaya Vijayan

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P2860

The Cancer Genome Atlas Pan-Cancer analysis project

VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing

Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia

A practical method to detect SNVs and indels from whole genome and exome sequencing data.

Detecting somatic point mutations in cancer genome sequencing data: a comparison of mutation callers

Comparison of somatic mutation calling methods in amplicon and whole exome sequence data.

Reducing INDEL calling errors in whole genome and exome sequencing data.

Combining calls from multiple somatic mutation-callers

SomaticSniper: identification of somatic point mutations in whole genome sequencing data

Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples.

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748

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scholarly article

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10.1186/S12864-017-4134-3

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English

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Suppl 7

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P478

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P577

2017-10-16T00:00:00Z

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29513195

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5657037

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