pestalotiopsis VS Sniffles

Compare pestalotiopsis vs Sniffles and see what are their differences.

pestalotiopsis

Assembly and phylogentic analysis pipeline for draft genome of a Pestalotiopsis fungi. (by EverymanBio)

Sniffles

Structural variation caller using third generation sequencing (by fritzsedlazeck)
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pestalotiopsis Sniffles
1 1
7 513
- -
0.0 7.7
about 2 years ago 8 days ago
Python Python
GNU General Public License v3.0 only GNU General Public License v3.0 or later
The number of mentions indicates the total number of mentions that we've tracked plus the number of user suggested alternatives.
Stars - the number of stars that a project has on GitHub. Growth - month over month growth in stars.
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pestalotiopsis

Posts with mentions or reviews of pestalotiopsis. We have used some of these posts to build our list of alternatives and similar projects. The last one was on 2021-12-26.
  • Sequencing your DNA with a USB dongle and open source code
    3 projects | news.ycombinator.com | 26 Dec 2021
    That's not true. I just did a high-quality sequence and assembly of a new species of fungus from my home lab using nanopore. You can see all my code used for assembly and analysis that will be referenced in a paper I plan to publish in Jan here: https://github.com/EverymanBio/pestalotiopsis

Sniffles

Posts with mentions or reviews of Sniffles. We have used some of these posts to build our list of alternatives and similar projects.

What are some alternatives?

When comparing pestalotiopsis and Sniffles you can also consider the following projects:

malware-phylogeny - malware phylogeny for WSO web shell, Shellbot IRC bot and algorithm

truvari - Structural variant toolkit for VCFs

MultiQC - Aggregate results from bioinformatics analyses across many samples into a single report.

fastp - An ultra-fast all-in-one FASTQ preprocessor (QC/adapters/trimming/filtering/splitting/merging...)

manta - Structural variant and indel caller for mapped sequencing data

pipeline-structural-variation - Pipeline for calling structural variations in whole genomes sequencing Oxford Nanopore data