Athurva Gore/LabNotes/2009-8-13: Difference between revisions
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** ZhangSNP (on opposite strand to target cDNA) | ** ZhangSNP (on opposite strand to target cDNA) | ||
** TDMR Set (Also check if out-of-memory happens again...maybe run on Miner?) | ** TDMR Set (Also check if out-of-memory happens again...maybe run on Miner?) | ||
=IPS and Cancer= | |||
* Used Dr. Zhang's scripts on lane 1 and lane 3. | |||
** Both lane 1 and lane 3 do not use size-selection, making them better comparisons. | |||
** This would imply that lane 2 is missing alleles...not sure why this might happen. | |||
* Took alleles present in Lane 1 in locations with differences; this allows analysis of homozygous->heterozygous SNPs (as this is what would be expected) | |||
** Should probably also look at heterozygous->homozygous, as this is possible...but probably want to ignore homozygous->homozygous | |||
** Data file is in genome-miner:/home/ajgore/ExomeReads/s1_vs_s3_variants.txt | |||
* Ran data through SIFT | |||
** SIFT found: | |||
Number of coding variants: 226 | |||
Coding variants predicted: 53% (122) | |||
Tolerated: 47% (58) | |||
Damaging: 53% (64) | |||
Nonsynonymous: 56% (127) | |||
Synonymous: 44% (99) | |||
Novel: 181% (222) | |||
* After looking at the genes, ONE GENE was found to be present in the Sanger Cancer Gene Census gene set | |||
** '''NTRK3''' | |||
** These genes have been implicated as being causative. | |||
* The COSMIC Gene set (Genes mutated in cancer, but not necessarily causative) was also analyzed | |||
** dfs |
Revision as of 22:21, 13 August 2009
NEW LAB NOTEBOOK NAVIGATION BAR
- Can now start each page with the following:
- {{ AGLabEntry|PREVIOUSDATE|NEXTDATE }}
- Where date format is YYYY-M-DD
Probe Generation
- DONE
- KKESH72
- CpG-SNP set (with 80 bp gap)
- CURRENTLY RUNNING:
- FlyDup901
- FlyDup936
- RPLCACRD
- FlyDup5279
- A-to-I Probes for Erez and Billy; currently generating list of sites near splice junctions
- Can then generate list of nearby exons and probes
- Then run through scripts as before
- TO RERUN:
- LeeCancer (on opposite strand to target cDNA)
- LeeXGenes (on opposite strand to target cDNA)
- ZhangSNP (on opposite strand to target cDNA)
- TDMR Set (Also check if out-of-memory happens again...maybe run on Miner?)
IPS and Cancer
- Used Dr. Zhang's scripts on lane 1 and lane 3.
- Both lane 1 and lane 3 do not use size-selection, making them better comparisons.
- This would imply that lane 2 is missing alleles...not sure why this might happen.
- Took alleles present in Lane 1 in locations with differences; this allows analysis of homozygous->heterozygous SNPs (as this is what would be expected)
- Should probably also look at heterozygous->homozygous, as this is possible...but probably want to ignore homozygous->homozygous
- Data file is in genome-miner:/home/ajgore/ExomeReads/s1_vs_s3_variants.txt
- Ran data through SIFT
- SIFT found:
Number of coding variants: 226 Coding variants predicted: 53% (122) Tolerated: 47% (58) Damaging: 53% (64) Nonsynonymous: 56% (127) Synonymous: 44% (99) Novel: 181% (222)
- After looking at the genes, ONE GENE was found to be present in the Sanger Cancer Gene Census gene set
- NTRK3
- These genes have been implicated as being causative.
- The COSMIC Gene set (Genes mutated in cancer, but not necessarily causative) was also analyzed
- dfs