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Hello all
I am a postdoc in the SF Bay and very pleased to join this fantastic forum. I am new to NGS but eager to learn, particularly about 454 and Illumina. I will be working primarily with two kinds of data: shotgun sequencing of mixed microbial communities with 454 and isolate sequencing with Illumina G2. I am particularly interested in methods to discover and validate SNPs in this data, as well as de novo and reference based aligners.
I am a postdoc in the SF Bay and very pleased to join this fantastic forum. I am new to NGS but eager to learn, particularly about 454 and Illumina. I will be working primarily with two kinds of data: shotgun sequencing of mixed microbial communities with 454 and isolate sequencing with Illumina G2. I am particularly interested in methods to discover and validate SNPs in this data, as well as de novo and reference based aligners.