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Top 14 Genome Open-Source Projects
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deepvariant
DeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.
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InfluxDB
Power Real-Time Data Analytics at Scale. Get real-time insights from all types of time series data with InfluxDB. Ingest, query, and analyze billions of data points in real-time with unbounded cardinality.
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DNABERT
DNABERT: pre-trained Bidirectional Encoder Representations from Transformers model for DNA-language in genome
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SaaSHub
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pyrodigal
Cython bindings and Python interface to Prodigal, an ORF finder for genomes and metagenomes. Now with SIMD!
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OSGenome
An Open Source Web Application for Genetic Data (SNPs) using 23AndMe and Data Crawling Technologies
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DIF
"DNA IMAGE FOOTPRINT" The main idea is to convert a DNA sequence to an image to find any related sequences in the image with common algorithms (by MahdiKarimian)
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Project mention: Calculating Average Coverage or Read Depth for a Sequence (WES) | /r/bioinformatics | 2023-06-24
If I want to get started, they said it's optional to pre-train (so you can skip to step 3). This is where I got tripped up: "Note that the sequences are in kmer format, so you will need to convert your sequences into that." From what I understand, you need to do this so that all of the sequences are the same length? So kmer=6 means all of the sequences are length 6? Someone suggested that I take the first nucleotide in the promoter and grab 3 nucleotides before and 3 nucleotides after (+/-3 bases). I don't think that's how the kmer thing works though? I tried replicating how I think it works down below (I got confused on the last row of the 'after' df). Please correct me if I'm wrong!
True! I believe bakta relies on this python implementation of prodigal for translation https://github.com/althonos/pyrodigal
Genome related posts
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Calculating Average Coverage or Read Depth for a Sequence (WES)
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How to get a DNA report using AncestryDNA/23andme raw data without uploading to another server?
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Why is bedtools genomecov giving me a blank output file?
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Nanopore long read assembly help!
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Cross-species functional annotation?
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Generate image footprint from DNA sequence for sequence matching
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Raw nanowire sequencer data
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A note from our sponsor - SaaSHub
www.saashub.com | 6 May 2024
Index
What are some of the best open-source Genome projects? This list will help you:
Project | Stars | |
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1 | deepvariant | 3,080 |
2 | mosdepth | 656 |
3 | DNABERT | 543 |
4 | Augustus | 264 |
5 | masurca | 229 |
6 | NanoSim | 213 |
7 | eager | 124 |
8 | pyrodigal | 122 |
9 | OSGenome | 107 |
10 | PGA | 46 |
11 | hmep | 7 |
12 | bioinformatics | 3 |
13 | Genome | 3 |
14 | DIF | 1 |
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