Dear all,
I am currently running tophat to align human genome reference(hg19 bowtie index) to illumina pair-end data of size 17Gb each(17*2)....
3 results in 0.0021 seconds.
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MAQ easyrun problem and questions.
Hello guys, your input are much appreciated.
I am running small RNA sequencing here and trying to compare MAQ and the Flicker from illumina. ... -
is my reference too big for maq?
I am trying to convert my reference fasta file to bfa using maq with the command fasta2bfa.
I am having a segmentation fault.
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