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Find chromosomal location of a scaffold

For two closely related species, is there an easy way to align genome assemblies?

Species A is a chromosomal assembly (although it has gaps) and Species B is assembled into smaller scaffolds. I would like to figure out where Species B scaffolds lie on the Species A assembly in order to leverage annotations that are available for A but not B.

Thank you very much!

genome mapping

1 answer

See this answer. You can also use bwa mem, minimap2, Blat, among others.

For annotation transfer, see RATT.

Thanks for the response. However, the answer and methods you refer me to have to do with mapping reads to a genome. What I'm interested in doing is aligning fasta genomes to each other (or rather, finding the chromosome location scaffold X corresponds with).

The question indeed is about mapping reads to a second reference genome, but no, the answer I linked is not about mapping reads to a genome, it is about aligning scaffolds to a complete genome:

Don't map the reads back to the Zebra Finch genome.

MUMmer is one of the programs commonly used for aligning contigs / scaffolds to reference genomes, and is a requirement for RATT, which is a software to transfer annotation from a reference (annotated) genome to an unannotated query genome.

edit: just to clarify, bwa mem, minimap2 and Blast are all also used for contig / scaffold mapping to a reference genome, with the requirement the reference genome should be close and reasonably similar to the query contig / scaffolds - I believe at most 10-15% difference, someone will correct me if I got the numbers wrong.

Thanks for the clarification!

I had indeed provided the wrong link, I linked to a comment to the answer I wanted to link. I've corrected it now.

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