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Comment: How to normalise RNA seq data from two independent experiments to the same scale
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Comment: Modify the code to take most abundant reads from a cluster and process it.
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Comment: Which minimap2 parameters to set while performing mapping to avoid such mismatch
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Comment: Which minimap2 parameters to set while performing mapping to avoid such mismatch
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Comment: How to discard alignments from SAM/BAM file that have mismatches
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Comment: How to discard alignments from SAM/BAM file that have mismatches
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Comment: minimap's SAM file MAPQ value for the unique alignments
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Comment: IGV grey vs white lines
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Comment: How to extract out gene specific reads from concatenated fastq file
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