ERVcaller is a tool designed to accurately detect and genotype non-reference unfixed endogenous retroviruses (ERVs) and other transposable elements (TEs) in the human genome using next-generation sequencing (NGS) data. We evaluated the tools using both simulated and real benchmark whole-genome sequencing (WGS) datasets. ERVcaller is capable to accurately detect various TE insertions of any lengths, particularly ERVs. It allows for the use of a TE reference library regardless of sequence complexity, such as the entire RepBase database. It is easy to install and use with command lines.
Hi there,
I would like to kindly inquire, if I input a BAM file that is aligned to 'GRCh38_full_analysis_set_plus_decoy_hla.fa', when executing 'ERVcaller_v1.4.pl', should the '-H' parameter input be 'GRCh38_full_analysis_set_plus_decoy_hla.fa', or should it still be the 'hg38.fa' without ALT contig?
I appreciate your guidance on this matter. Thank you.
Hi there, I would like to kindly inquire, if I input a BAM file that is aligned to 'GRCh38_full_analysis_set_plus_decoy_hla.fa', when executing 'ERVcaller_v1.4.pl', should the '-H' parameter input be 'GRCh38_full_analysis_set_plus_decoy_hla.fa', or should it still be the 'hg38.fa' without ALT contig? I appreciate your guidance on this matter. Thank you.