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How to map billions of short reads onto genomes

scientific article (publication date: May 2009)

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How to map billions of short reads onto genomes (English)

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Steven L Salzberg

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Cole Trapnell

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Cole Trapnell

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English

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publication date

May 2009

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published in

Nature Biotechnology

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volume

27

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issue

5

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page(s)

455-7

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cites work

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20 March 2017

Ultrafast and memory-efficient alignment of short DNA sequences to the human genome

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PubMed Central

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20 March 2017

Annotating genomes with massive-scale RNA sequencing

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20 March 2017

DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome

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20 March 2017

Alternative isoform regulation in human tissue transcriptomes

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20 March 2017

Mapping short DNA sequencing reads and calling variants using mapping quality scores

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20 March 2017

Mapping and quantifying mammalian transcriptomes by RNA-Seq

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20 March 2017

The transcriptional landscape of the yeast genome defined by RNA sequencing

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20 March 2017

Deep surveying of alternative splicing complexity in the human transcriptome by high-throughput sequencing

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PubMed Central

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7 April 2017

Genome-wide mapping of in vivo protein-DNA interactions

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PubMed Central

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retrieved

7 April 2017

Identifiers

DOI

10.1038/NBT0509-455

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1756379

OpenCitations bibliographic resource ID

1756379

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1756379

PMC publication ID

2836519

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PubMed publication ID

19430453

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ResearchGate publication ID

24416031

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(Q28244503)

How to map billions of short reads onto genomes

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