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2.5 years ago
andrebolerbarros
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0
Hi everyone,
I have samples which align with two different genomes with a great degree of similarity. Is there any way to handle/correct/take into consideration reads that align to two genomes?
Currently, I'm working on DEG using R and DESeq2.
Thanks in advance
Sounds like these are
xenograft(type) datasets, if not for mouse/human. Considerations like this can still apply. An example paper :https://bmcmedgenomics.biomedcentral.com/articles/10.1186/s12920-019-0551-2
https://www.nature.com/articles/s41467-021-25177-3
That's a very good suggestion, hadn't thought about it. Thanks!