Open mpoelchau opened 3 years ago
We are exploring moving to cram format from bam to save space. @debbiedai can you create a new branch that does the following:
add samtools view input.bam -o <output.cram> -C -T <genome.fasta> --level=9 to RNAseq_annotate.py. The input bam file would be from here: https://github.com/NAL-i5K/NAL_RNA_seq_annotation_pipeline/blob/master/rnannot/RNAseq_annotate.py#L518
samtools view input.bam -o <output.cram> -C -T <genome.fasta> --level=9
Rename the cram output file in the same style as https://github.com/NAL-i5K/NAL_RNA_seq_annotation_pipeline/blob/master/rnannot/RNAseq_annotate.py#L532
Add the cram file to add_trackList.py (I need to provide more information on how to add to the trackList.json file)
Remove the bam file and bam.bai file information from add_trackList.py
We are exploring moving to cram format from bam to save space. @debbiedai can you create a new branch that does the following:
add
samtools view input.bam -o <output.cram> -C -T <genome.fasta> --level=9
to RNAseq_annotate.py. The input bam file would be from here: https://github.com/NAL-i5K/NAL_RNA_seq_annotation_pipeline/blob/master/rnannot/RNAseq_annotate.py#L518Rename the cram output file in the same style as https://github.com/NAL-i5K/NAL_RNA_seq_annotation_pipeline/blob/master/rnannot/RNAseq_annotate.py#L532
Add the cram file to add_trackList.py (I need to provide more information on how to add to the trackList.json file)
Remove the bam file and bam.bai file information from add_trackList.py