n00c's profile

Recent Activity

• 23:05: posted Simultaneous alignment of short reads against multiple genomes
• 22:59: posted What would you do if you could sequence everything?
• 22:59: posted Cheap third-generation sequencing
• 22:47: posted Initial sequencing and analysis of the human genome

• 10:47: added a note to Genome sequencing in microfabricated high-density picolitre reactors
• 09:37: posted Genome sequencing in microfabricated high-density picolitre reactors
• 00:07: posted Supplementary Information - Pyrobayes: an improved base caller for SNP discovery in pyrosequences

• 21:12: posted sff_extract
• 20:36: posted Standard Flowgram Format (SFF)

• 20:57: posted Nature Protocols: Genome resequencing and identification of variations by Illumina Genome Analyzer Reads
• 20:54: posted Searching for SNPs with cloud computing

• 22:33: posted BFAST: An Alignment Tool for Large Scale Genome Resequencing

• 23:18: added a note to The first Korean genome sequence and analysis: Full genome sequencing for a socio-ethnic group
• 23:17: added a note to A highly annotated whole-genome sequence of a Korean individual

• 23:28: posted Comprehensive resequence analysis of a 97 kb region of chromosome 10q11.2 containing the MSMB gene associated with prostate cancer