PANDAseq: paired-end assembler for illumina sequences.
PANDAseq: paired-end assembler for illumina sequences.
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DOI:
10.1186/1471-2105-13-31
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发表时间:
2012-02-14
影响因子:
3
通讯作者:
Neufeld JD
中科院分区:
文献类型:
--
作者:
Masella AP;Bartram AK;Truszkowski JM;Brown DG;Neufeld JD
Illumina paired-end reads are used to analyse microbial communities by targeting amplicons of the 16S rRNA gene. Publicly available tools are needed to assemble overlapping paired-end reads while correcting mismatches and uncalled bases; many errors could be corrected to obtain higher sequence yields using quality information. PANDAseq assembles paired-end reads rapidly and with the correction of most errors. Uncertain error corrections come from reads with many low-quality bases identified by upstream processing. Benchmarks were done using real error masks on simulated data, a pure source template, and a pooled template of genomic DNA from known organisms. PANDAseq assembled reads more rapidly and with reduced error incorporation compared to alternative methods. PANDAseq rapidly assembles sequences and scales to billions of paired-end reads. Assembly of control libraries showed a 4-50% increase in the number of assembled sequences over naïve assembly with negligible loss of "good" sequence.
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影响因子:
4.4
作者:
Bartram, Andrea K.;Lynch, Michael D. J.;Neufeld, Josh D.
通讯作者:
Neufeld, Josh D.
影响因子:
14.9
作者:
Cole JR;Wang Q;Cardenas E;Fish J;Chai B;Farris RJ;Kulam-Syed-Mohideen AS;McGarrell DM;Marsh T;Garrity GM;Tiedje JM
通讯作者:
Tiedje JM
DOI:
10.1073/pnas.1000080107
发表时间:
2011-03-15
影响因子:
11.1
作者:
Caporaso, J. Gregory;Lauber, Christian L.;Knight, Rob
通讯作者:
Knight, Rob
影响因子:
14.9
作者:
Cock PJ;Fields CJ;Goto N;Heuer ML;Rice PM
通讯作者:
Rice PM
影响因子:
14.9
作者:
Cole JR;Chai B;Farris RJ;Wang Q;Kulam-Syed-Mohideen AS;McGarrell DM;Bandela AM;Cardenas E;Garrity GM;Tiedje JM
通讯作者:
Tiedje JM