SeqPurge: highly-sensitive adapter trimming for paired-end NGS data
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[1] Helga Thorvaldsdóttir,et al. Integrative Genomics Viewer , 2011, Nature Biotechnology.
[2] Marcel Martin. Cutadapt removes adapter sequences from high-throughput sequencing reads , 2011 .
[3] Björn Usadel,et al. Trimmomatic: a flexible trimmer for Illumina sequence data , 2014, Bioinform..
[4] Matthew D. Wilkerson,et al. ABRA: improved coding indel detection via assembly-based realignment , 2014, Bioinform..
[5] Jui-Hung Hung,et al. PEAT: an intelligent and efficient paired-end sequencing adapter trimming algorithm , 2015, BMC Bioinformatics.
[6] Stinus Lindgreen,et al. AdapterRemoval: easy cleaning of next-generation sequencing reads , 2012, BMC Research Notes.
[7] Alexa B. R. McIntyre,et al. Extensive sequencing of seven human genomes to characterize benchmark reference materials , 2015, Scientific Data.
[8] Shuifang Zhu,et al. Skewer: a fast and accurate adapter trimmer for next-generation sequencing paired-end reads , 2014, BMC Bioinformatics.
[9] Martin Goodson,et al. Stampy: a statistical algorithm for sensitive and fast mapping of Illumina sequence reads. , 2011, Genome research.
[10] Gabor T. Marth,et al. Haplotype-based variant detection from short-read sequencing , 2012, 1207.3907.
[11] Heng Li. Aligning sequence reads, clone sequences and assembly contigs with BWA-MEM , 2013, 1303.3997.
[12] M. Morgante,et al. An Extensive Evaluation of Read Trimming Effects on Illumina NGS Data Analysis , 2013, PloS one.