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Hello, we find some discrepancies between our final polished genome assembly and cytogenetic map.
The main problem is that 3 chromosomes and several other genomic blocks (belonging to other chromosomes) are merged into one very large scaffold.
I tried several combinations of hicstuff parameters (different mapping software: bowtie2, bwa, minimap2; different mapping options: “iterative” or “cutsite”; the “duplicates” option to remove PCR artefacts), and finally run Instagraal using “-l 5” or “-l 5 -c 0” parameters. However, I always find this super scaffold.
Do you have any idea of what I could try to be more “stringent” and avoid that different chromosomes are merged together?
Thank you in advance!
The text was updated successfully, but these errors were encountered:
Hello, we find some discrepancies between our final polished genome assembly and cytogenetic map.
The main problem is that 3 chromosomes and several other genomic blocks (belonging to other chromosomes) are merged into one very large scaffold.
I tried several combinations of hicstuff parameters (different mapping software: bowtie2, bwa, minimap2; different mapping options: “iterative” or “cutsite”; the “duplicates” option to remove PCR artefacts), and finally run Instagraal using “-l 5” or “-l 5 -c 0” parameters. However, I always find this super scaffold.
Do you have any idea of what I could try to be more “stringent” and avoid that different chromosomes are merged together?
Thank you in advance!
The text was updated successfully, but these errors were encountered: