Hi, I'm new to genomic data and I'm just learning the basics of Illumina HiSeq and the resulting data. There's one thing I'm confused about.
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basic Q about paired end reads from HiSeq
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Sequence Coverage and Genome Insertion lenght from SAM
Hi to everyone,
I'm quite new of this science, and I'm looking for solve a problem.
I've a SAM file generated by BWA and... -
Extracting insert size from .bam using pysam
Hi there, this is my first time posting. I am fairly new to bioinformatics so I may make silly errors here and there.
Anyway, I have been... -
lots of overlapping reads - Pair-end library from Nextera
We have done a couple of run (2X150 and 2X250) of Miseq on bacteria genome sequencing. They all have a high overlapping rate (>80%).
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