QQ-SNV: single nucleotide variant detection at low frequency by comparing the quality quantiles.

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QQ-SNV: single nucleotide variant detection at low frequency by comparing the quality quantiles.

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2015 nî lūn-bûn

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2015年論文

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QQ-SNV: single nucleotide vari ...... mparing the quality quantiles.

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QQ-SNV: single nucleotide vari ...... mparing the quality quantiles.

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QQ-SNV: single nucleotide vari ...... mparing the quality quantiles.

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QQ-SNV: single nucleotide vari ...... mparing the quality quantiles.

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QQ-SNV: single nucleotide vari ...... mparing the quality quantiles.

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QQ-SNV: single nucleotide vari ...... mparing the quality quantiles.

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P1476

QQ-SNV: single nucleotide vari ...... mparing the quality quantiles.

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Bie Verbist

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Herman van Vlijmen

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Jeroen Aerssens

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Kim Thys

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Koen Van der Borght

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Lieven Clement

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Yves Wetzels

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P2860

The Sanger FASTQ file format for sequences with quality scores, and the Solexa/Illumina FASTQ variants

Sequencing technologies - the next generation

The Sequence Alignment/Map format and SAMtools

Pyrosequencing sheds light on DNA sequencing

Challenges and opportunities in estimating viral genetic diversity from next-generation sequencing data

A framework for variation discovery and genotyping using next-generation DNA sequencing data

ReQON: a Bioconductor package for recalibrating quality scores from next-generation sequencing data.

Tools for mapping high-throughput sequencing data.

ViVaMBC: estimating viral sequence variation in complex populations from illumina deep-sequencing data using model-based clustering

Identification and correction of systematic error in high-throughput sequence data

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s12859-015-0812-9

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scholarly article

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10.1186/S12859-015-0812-9

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Joke Reumers

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2015-11-10T00:00:00Z

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283718351

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