Very useful! I refined these sequences. Hopes they're clearer. Genomic DNA Adapter: 5' -------------------- -----ACACTCTTTCCCTAC ACGACGCTCTTCCGATCT (-) -------------------- -------------- 3' 3' -------------------- -----TGTGAGAAAGGGATG TGCTGCGAGAAGGCTAGp (-) -------------------- -------------- 5' Adapter: 5' -------------------- -------------------- ------------------ (-) pGATCGGAAGAGCTCGTATG CCGT
"Also how do you define a duplicate?" As you suggest, this can be done in at least two ways. Both have caveats. If you define duplicates as reads with identical sequence you may underestimate the presence of duplicates in your library. Read errors present in your library will result in reads with apparently different sequences that could have actually come from PCR amplifications of the same cDNA
Hello everyone! I am here collecting the information of browsers/viewers especially for RNA sequencing data, which can mainly show the gene annotation track, read track (including spliced reads), and some other annotation tracks. This is the basic requirment of RNA-seq data viewing. Thanks to the Seqanswers wiki page, I listed the browsers/viewers for RNA-seq below. But due to my limited experienc
28 Dec 2009: This thread has been closed. Please see our wiki software portal for information about each of these packages. A reasonably thorough table of next-gen-seq software available in the commercial and public domain Integrated solutions * CLCbio Genomics Workbench - de novo and reference assembly of Sanger, Roche FLX, Illumina, Helicos, and SOLiD data. Commercial next-gen-seq software that
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