-
Notifications
You must be signed in to change notification settings - Fork 42
New issue
Have a question about this project? Sign up for a free GitHub account to open an issue and contact its maintainers and the community.
By clicking “Sign up for GitHub”, you agree to our terms of service and privacy statement. We’ll occasionally send you account related emails.
Already on GitHub? Sign in to your account
Realignment using assembly to pick variants #200
Comments
fnothaft
added a commit
to fnothaft/avocado
that referenced
this issue
Jan 23, 2017
Resolves bigdatagenomics#200. Depends on bigdatagenomics/adam#1363. * Adds a ConsensusRealigner that uses the main Realigner to realign reads, which are then fed into the variant discovery engine with loose filters. Any INDEL variants that are discovered are then fed in to ADAM's INDEL realignment engine as known INDELs. * Uses this realignment mode in the BiallelicGenotyperSuite to clean up a previously failing test. * Adds this to the Reassemble CLI as a `-use_consensus_realigner` switch.
fnothaft
added a commit
to fnothaft/avocado
that referenced
this issue
Jan 25, 2017
Resolves bigdatagenomics#200. Depends on bigdatagenomics/adam#1363. * Adds a ConsensusRealigner that uses the main Realigner to realign reads, which are then fed into the variant discovery engine with loose filters. Any INDEL variants that are discovered are then fed in to ADAM's INDEL realignment engine as known INDELs. * Uses this realignment mode in the BiallelicGenotyperSuite to clean up a previously failing test. * Adds this to the Reassemble CLI as a `-use_consensus_realigner` switch.
fnothaft
added a commit
to fnothaft/avocado
that referenced
this issue
Feb 28, 2017
Resolves bigdatagenomics#200. Depends on bigdatagenomics/adam#1363. * Adds a ConsensusRealigner that uses the main Realigner to realign reads, which are then fed into the variant discovery engine with loose filters. Any INDEL variants that are discovered are then fed in to ADAM's INDEL realignment engine as known INDELs. * Uses this realignment mode in the BiallelicGenotyperSuite to clean up a previously failing test. * Adds this to the Reassemble CLI as a `-use_consensus_realigner` switch.
fnothaft
added a commit
to fnothaft/avocado
that referenced
this issue
Mar 1, 2017
Resolves bigdatagenomics#200. Depends on bigdatagenomics/adam#1363. * Adds a ConsensusRealigner that uses the main Realigner to realign reads, which are then fed into the variant discovery engine with loose filters. Any INDEL variants that are discovered are then fed in to ADAM's INDEL realignment engine as known INDELs. * Uses this realignment mode in the BiallelicGenotyperSuite to clean up a previously failing test. * Adds this to the Reassemble CLI as a `-use_consensus_realigner` switch.
Sign up for free
to join this conversation on GitHub.
Already have an account?
Sign in to comment
We should use the assembly code to pick out INDEL variants that are then thrown into the ADAM indel realigner's "known INDELs" mode.
The text was updated successfully, but these errors were encountered: