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
[email protected]
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
[email protected]