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Answer to biostar https://www.biostars.org...
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My answer to https://www.biostars.org/p/138848/ Question: How to replace a set of sequence ID's with another set of sequence ID's ?? Let us consider I have a file (Notepad or MS-doc) having 10 sequences with ID's A, B, C, D, E, F, G, H, I, J. I want to replace the ID's with K, L, M, N, O ,P, Q, R, S, T i.e., A to re replaced with K, B to be replaced with M and so on. How can I do this? I am a Biologist who have newly started analyzing Large data's and having this prob...
Created: 2015-04-20
| Last updated: 2015-04-20
Credits:
PL
The NOTCH2 workflow
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Analysis of the exome sequencing data for the following article:
Nat Genet. 2011 Mar 6;43(4):306-8.
Truncating mutations in the last exon of NOTCH2 cause a rare skeletal disorder with osteoporosis.
Isidor B, Lindenbaum P, Pichon O, Bézieau S, Dina C, Jacquemont S, Martin-Coignard D, Thauvin-Robinet C, Le Merrer M, Mandel JL, David A, Faivre L, Cormier-Daire V, Redon R, Le Caignec C.
using knime4bio
Created: 2011-09-06
| Last updated: 2011-09-06
Credits:
PL
Query dbsnp, transform to HTML
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This is a XProc worklow. Its input is a list of Entrez queries packed in a html list:
See http://plindenbaum.blogspot.com/2009/05/xml-pipelines-xproc-for-bioinformatics.html
"snp_gene_clin"[Filter] AND "snp_pubmed_cited"[Filter] AND 2[CHR]
(1000[CHRPOS] : 5000[CHRPOS]) AND 2[CHR] AND "homo sapiens"[Organism]
it queries entrez, download the SNPs as XML and transform the result as an HTML table:
r...
Created: 2009-05-21
| Last updated: 2009-05-21
Credits:
PL
snpNeighbours
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My first Taverna workflow: the input is the SNP "rs25". The Web Services invoked finds its position on the human genome and find its neighbours at 100bp. The XML result is then saved to a local file. The web services used here are under developpement and might be turned off in a near future.
Created: 2009-05-14
| Last updated: 2009-05-14
Credits:
PL