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.
Dear ERVcaller team,
Hi, I'm Oh.
Thanks for your program.
Then, I have a question.
Can I use GATK pre-processed bam files for input bam of ERVcaller?
I have only pre-processed bam files. In this text, pre-processing means sorting, marking duplicate reads, and recalibrating (https://gatk.broadinstitute.org/hc/en-us/articles/360035535912-Data-pre-processing-for-variant-discovery).
Many Thanks.
Oh.