Dear all, I've been trying to test if I can produce the same fusion call starting from BAM instead of FASQ. My STAR command is as such.
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5 results in 0.0026 seconds.
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BAM -> FASTQ why can I not produce the same result?
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How to Print Statistics from Python filtering script
Hello all,
I have the following python script which will filter paired-end fastq read data based on nucleotide complexity with a user... -
Chip-seq analyse using USeq
hi, i have a problem
this is the first time i analyse Chip seq data and i have the following problem:
i received my fastq... -
Chip-seq analyse using USeq
hi, i have a problem
this is the first time i analyse Chip seq data and i have the following problem:
i received my fastq... -
fastq to fasta conversion
How can I convert my fastq files to two fasta files with one containing the reads and another containing the quality scores?
Thanks :c...
