sv-callers

Snakemake-based workflow for detecting structural variants in genomic data (by GooglingTheCancerGenome)

Sv-callers Alternatives

Similar projects and alternatives to sv-callers

NOTE: The number of mentions on this list indicates mentions on common posts plus user suggested alternatives. Hence, a higher number means a better sv-callers alternative or higher similarity.

sv-callers reviews and mentions

Posts with mentions or reviews of sv-callers. We have used some of these posts to build our list of alternatives and similar projects. The last one was on 2023-03-28.
  • Do you know how to get CNVs out of WES data sorted.bam files? (Free)
    2 projects | /r/bioinformatics | 28 Mar 2023
    Generally, you have multiple ways to tackle this kind of a problem. For short read sequencing you have two types of CNV detection - readdepth based and paired-end based. CNVpytor (CNVnator) for example, is the former. You also have manta and lumpy. A lot of good pipelines use more than one SV caller and integrate them. For example: https://github.com/GooglingTheCancerGenome/sv-callers

Stats

Basic sv-callers repo stats
1
71
2.9
3 months ago

GooglingTheCancerGenome/sv-callers is an open source project licensed under Apache License 2.0 which is an OSI approved license.

The primary programming language of sv-callers is Python.


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