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Lots of unmapped reads - SOLiD bacterial RNA-seq and bowtie mapping
(Topic in the RNA Sequencing forum)
01-17-2013, 12:11 PM
Low number of variants taken from high GB data- NextSeq 500
(Topic in the Introductions forum)
06-21-2017, 03:48 AM
Make a complete genome sequences from Illumina data
(Topic in the Illumina (Solexa) forum)
08-30-2011, 05:58 PM
Map 454 RNA-seq single-end reads on a genome: UPDATE
(Topic in the Bioinformatics forum)
05-16-2014, 03:36 AM
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