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#1 |
Member
Location: Brazil - Belo Horizonte - UFMG Join Date: Jan 2011
Posts: 14
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Good Morning.
My name's André Horta, i'm from Brazil, i'm doing pós-doc in Molecular Medicine at UFMG. I follow the instructions (http://cbcb.umd.edu/software/BRCA-diagnostic/), and everything it's aright. I have generates two files, brca1.coverage, brca2.coverage, brca1.report and brca2.report. But, the question is, what do i do with this files? What's represent? I caught the genome from the "1000 genome project" (ftp://ftp-trace.ncbi.nih.gov/1000gen...sequence_read/) and i was used SRA toolkit to convert lite.sra to fastq (http://www.ncbi.nlm.nih.gov/books/NBK50846/) and use BRCA-DIAGNOSTIC. I need your help, i was confused. Thank you very much! André Horta andrehorta1g@gmail.com |
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Tags |
brca, diagnostic, dna, linux, sequencing |
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