FastUniq: a fast de novo duplicates removal tool for paired short reads (Q34533452)

2 August 2017

title

FastUniq: a fast de novo duplicates removal tool for paired short reads (English)

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2 August 2017

8

Shilin Chen

1 reference

2 August 2017

Haibin Xu

1

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2 August 2017

Xiang Luo

2

1 reference

2 August 2017

Jun Qian

3

1 reference

2 August 2017

Xiaohui Pang

4

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2 August 2017

Jingyuan Song

5

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2 August 2017

Guangrui Qian

6

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2 August 2017

Jinhui Chen

7

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2 August 2017

language of work or name

English

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publication date

20 December 2012

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2 August 2017

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2 August 2017

volume

7

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2 August 2017

issue

12

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2 August 2017

page(s)

e52249

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Creative Commons Attribution 4.0 International

2 August 2017

copyright license

start time

20 December 2012

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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7 July 2018

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7 July 2018

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Performance comparison of exome DNA sequencing technologies

7 July 2018

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7 July 2018

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Using the Acropora digitifera genome to understand coral responses to environmental change

7 July 2018

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SEAL: a distributed short read mapping and duplicate removal tool

7 July 2018

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A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement

7 July 2018

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7 July 2018

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Quality control procedures for genome-wide association studies

7 July 2018

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7 July 2018

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Scaffolding pre-assembled contigs using SSPACE

7 July 2018

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Function annotation of the rice transcriptome at single-nucleotide resolution by RNA-seq

7 July 2018

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Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing

7 July 2018

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Population genomics of parallel adaptation in threespine stickleback using sequenced RAD tags

7 July 2018

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De novo assembly of human genomes with massively parallel short read sequencing

7 July 2018

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The sequence and de novo assembly of the giant panda genome

7 July 2018

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Mu transposon insertion sites and meiotic recombination events co-localize with epigenetic marks for open chromatin across the maize genome

7 July 2018

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Searching for SNPs with cloud computing

7 July 2018

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7 July 2018

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Fast and accurate short read alignment with Burrows-Wheeler transform

7 July 2018

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Comparative analysis of Alu repeats in primate genomes

7 July 2018

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Amplification-free Illumina sequencing-library preparation facilitates improved mapping and assembly of (G+C)-biased genomes

7 July 2018

1 reference

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7 July 2018

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7 July 2018

1 reference

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Paired-end mapping reveals extensive structural variation in the human genome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3527383

An initial map of insertion and deletion (INDEL) variation in the human genome.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3527383

Comparison of DNA sequences with protein sequences.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3527383

High-throughput oncogene mutation profiling in human cancer

7 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0052249

10.1371/JOURNAL.PONE.0052249

21 January 2018

Identifiers

DOI

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2 August 2017

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2 August 2017

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