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Hello, Stephen.
Thank you for your follow-up question.
Since the ADNI data seems to have rsIDs, the recommended method would be to use a list of rsIDs to convert the coordinates between assemblies. Since you want ADNI data (hg18) to match the SNP 151 Common (hg38), you can use the Table Browser. For example, if you have a list like the following:
You can then navigate to the Table Browser (http://genome.ucsc.edu/cgi-bin/hgTables) and make the following selections:
1.
clade: Mammal
genome: Human
assembly: Dec. 2013 (GRCh38/hg38)
group: Variation
track: Common SNPs(151)
table: snp151Common
2. Set the region to “genome”.
3. Click paste list next to “identifiers (names/accessions):” and enter your list of rsIDs. Then click submit. You may get a message of rsIDs having no match in the snp151Common table.
4. Set the output format to “Selected fields from primary and related tables”. This will allow you to select fields of interest.
5. Insert a name next to “output filename:”, such as rsIDs_snp151Common_hg38.
6. Click get output.
7. On the Select Fields from hg38.snp151Common page, select “chrom”, “chromStart”, “chromEnd”, and “name” fields. Click get output.
8. The output will give you the coordinates and the rsIDs for SNP 151 Common on hg38.
We do offer Common dbSNP(153) and Common dbSNP(155) on hg38, where the datasets are formatted as bigBed files instead of MariaDb tables. For these datasets, you could use the bigBedNamedItems command-line tool to extract the rsID coordinates, similar to the Table Browser steps. We updated our FAQ to make it more clear:
https://genome.ucsc.edu/FAQ/FAQreleases.html#snpConversion
I hope this is helpful. If you have any further questions, please reply to gen...@soe.ucsc.edu. All messages sent to that address are archived on a publicly-accessible Google Groups forum. If your question includes sensitive data, you may send it instead to genom...@soe.ucsc.edu.
Gerardo Perez
UCSC Genomics Institute
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