<p>Hello</p> <p>Here are a few lines from the watson snp data in gff format:</p> <pre><code>#chr1 JW genotype 42101 42101 . + . SNP rs2691277.1;alleles T/G;ref_allele …
<p>Hi</p> <p>I will post this question to the ensembl mailing list but i thought i would try this forum too.</p> <p>ensembl variation database has the …
<p>Hello</p> <p>dbSNP makes the distinction between snps which are classed as chUn (variations on unplaced chromosomes) and chNotOn (variations which aren't mapped to any chromosomes)</p> …
<p>Wise bioinformaticians</p> <p>Please can you clarify something for me regarding dbSNP. I know dbSNP stores lots of different types of variations but lets just use …
<p>Hello</p> <p>I don't understand the results returned by dbSNP. I have read their user manual and whilst it explains some things very well, it seems …
<p>Venerable bioinformaticians,</p> <p>Please can you help me.</p> <p>How do i find out which version of dbSNP is used by a particular version of ensembl.</p> <p>For …
Hi Gary, Welcome on biostar. By chance, your question has already been answered before.
Hi Pierre, I'm afraid I can't find the earlier question after searching for a few mins. Do you have a link? Thanks.
Sorry, I am new to Biostar. How, exactly, would I find the answer to this question? None of the search terms that occur to me are any help.
Sorry, the previous URL was not recorded when I closed the question. The URL is Multiple Entries With The Same Rs Number In Dbsnp131
Thanks for the link. However, the dbSNP mapping process manual does not address how an rs number can be duplicated on two different chromosomes.
Why? See the segmental duplications in the UCSC genome browser: