I am currently working with whole-genome alignments generated using Cactus. I used phastCons to predict conserved elements and then employed phyloP to detect lineage-specific accelerated elements based on these conserved elements. However, when trying to retrieve the original sequence information from the whole-genome alignments (in MAF format) using these detected accelerated elements' coordinates (with the human reference), I couldn't find all corresponding FASTA sequences.
These accelerated elements were identified based on MAF files generated through the cactus-hal2maf process. Upon manually checking the missing regions, I discovered that some elements, which were marked as accelerated by phyloP, do not have corresponding sequence information in the MAF files. Despite this absence, phyloP identified these regions as accelerated.
I intend to use these original sequences for downstream analyses, such as the phyloacc workflow, but I am facing difficulties in finding the sequences for some detected accelerated elements. I would like to understand at which step I might be going wrong or missing crucial settings.
Hello,
I am currently working with whole-genome alignments generated using Cactus. I used phastCons to predict conserved elements and then employed phyloP to detect lineage-specific accelerated elements based on these conserved elements. However, when trying to retrieve the original sequence information from the whole-genome alignments (in MAF format) using these detected accelerated elements' coordinates (with the human reference), I couldn't find all corresponding FASTA sequences.
These accelerated elements were identified based on MAF files generated through the cactus-hal2maf process. Upon manually checking the missing regions, I discovered that some elements, which were marked as accelerated by phyloP, do not have corresponding sequence information in the MAF files. Despite this absence, phyloP identified these regions as accelerated.
I intend to use these original sequences for downstream analyses, such as the phyloacc workflow, but I am facing difficulties in finding the sequences for some detected accelerated elements. I would like to understand at which step I might be going wrong or missing crucial settings.
Thank you very much for your help!