Ido Tamir ★ 5.2k
Role: Moderator
Status: Active
Reputation: 5170
Joined: 10.2 years ago
Last seen: 5 weeks ago
Location: Austria

Tired of missing provenance for your fastq files?

Not knowing which scales the qualities are on?

 

Handling two files for paired end reads instead of one?

 

 

Try bam files instead! A well defined specification (for biological standards). Easy to use tools.

 

Convert illumina basecalls to bam files fresh from the machine: illumina2bam https://github.com/gq1/illumina2bam

 

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