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This repository has been archived by the owner on Mar 16, 2022. It is now read-only.
I'm still confused about what to do after running the pipeline. I've ran FALCON-unzip pipeline which including quiver to call high quality consensus. I got the cns_output/cns_p_ctg.fastq and cns_h_ctg.fastq.
My questions:
if a haplotigs is within a primary contig, that means sequences in the haplotigs represent one haplotype and the primary contig represent the other haplotype?
What would be the best way to proceed? I was hoping to get two sets of fasta files for each of the haplotype that I can used to map RNA-seq data to identify allele-specific expression.
Thank you!
The text was updated successfully, but these errors were encountered:
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I'm still confused about what to do after running the pipeline. I've ran FALCON-unzip pipeline which including quiver to call high quality consensus. I got the cns_output/cns_p_ctg.fastq and cns_h_ctg.fastq.
My questions:
Thank you!
The text was updated successfully, but these errors were encountered: