freebayes | Bayesian haplotype-based genetic polymorphism discovery | Genomics library
kandi X-RAY | freebayes Summary
kandi X-RAY | freebayes Summary
freebayes is a Bayesian genetic variant detector designed to find small polymorphisms, specifically SNPs (single-nucleotide polymorphisms), indels (insertions and deletions), MNPs (multi-nucleotide polymorphisms), and complex events (composite insertion and substitution events) smaller than the length of a short-read sequencing alignment.
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Trending Discussions on freebayes
QUESTION
I'm trying to filter on a condition that at least one of three columns has a value other than "".
My code works on a data.frame (or tibble), but on a raw DBI table I get an error:
...Error: Unknown input type: pairlist
ANSWER
Answered 2021-Jan-15 at 08:47Turns out only #3 (from below) works on DBI tables.
QUESTION
I have a workflow that requires an embarrassingly parallel step with different resource requirements (memory and time) for a slurm cluster. I decorated the workflow as per documentation:
...ANSWER
Answered 2021-Jan-08 at 11:52I have just noticed what I was doing wrong. My cluster.json was overriding the request because of the following line:
QUESTION
After running the variant calling, I would like to merge only specific outputs as shown in d
.
This is giving me an error of missing input files
. How to solve this?
ANSWER
Answered 2020-Oct-21 at 15:30The output of varcall
is
QUESTION
I installed the package in the following way:
...ANSWER
Answered 2019-Feb-09 at 22:40I think it should be:
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