Alternatives and similar repositories for pyladies-7:

Users that are interested in pyladies-7 are comparing it to the libraries listed below

• messa / pyladies-courseware
  Homework/task submit and review web app · based on React and Python aiohttp
  ☆18Updated 2 weeks ago
• PyLadiesCZ / pyladies.cz
  Website of the Czech PyLadies chapter / Web českých PyLadies
  ☆44Updated this week
• pyvec / naucse.python.cz
  Website with learning materials / Stránka s učebními materiály
  ☆325Updated this week
• PyLadiesCZ / pyladies
  Deprecated Website of the Czech PyLadies chapter / Starý web českých PyLadies
  ☆15Updated 5 years ago
• pyvec / cheatsheets
  Reference handouts / Taháky
  ☆36Updated 3 years ago
• LQYoLH / CnnCrispr
  A deep learning method for sgRNA off-target propensity prediction.
  ☆14Updated 4 years ago
• hsadasivan / mm2-ax
  ☆16Updated last year
• SAMtoBAM / PhasedDiploidGenomeAssemblyPipeline
  Using de-novo assembly and read-phasing to assemble reference-free diploid genomes
  ☆19Updated this week
• tomasbedrich / skoleni-python
  Materiály pro školení Základy Pythonu 3.
  ☆23Updated 2 years ago
• CMU-SAFARI / RawHash
  RawHash can accurately and efficiently map raw nanopore signals to reference genomes of varying sizes (e.g., from viral to a human genome…
  ☆52Updated 2 months ago
• btjaden / Rockhopper
  For computational analysis of bacterial RNA-seq data
  ☆10Updated 7 years ago
• Runsheng / trackcluster
  An analysis pipeline for Nanopore direct-RNA sequencing
  ☆12Updated 2 months ago
• bcgsc / straglr
  Tandem repeat expansion detection or genotyping from long-read alignments
  ☆93Updated 2 weeks ago
• kn-bibs / dotplot
  Simple visualisation tool for sequences' similarity in bioinformatics
  ☆13Updated 6 years ago
• Xinglab / TideHunter
  TideHunter: efficient and sensitive tandem repeat detection from noisy long reads using seed-and-chain
  ☆20Updated 8 months ago
• nanoporetech / pyguppyclient
  Python client library for Guppy
  ☆31Updated 2 years ago
• nanoporetech / sloika
  Sloika is Oxford Nanopore Technologies' software for training neural network models for base calling
  ☆25Updated 2 years ago
• MindAI / kmer
  A Python code for generating k-mer features for a set of DNA/ genomic sequences.
  ☆28Updated 6 months ago
• LooseLab / minotourapp
  Minotour API, web and client code
  ☆29Updated 2 years ago
• comprna / RATTLE
  Reference-free reconstruction and error correction of transcriptomes from Nanopore long-read sequencing
  ☆57Updated last year
• JustinChu / JupiterPlot
  A Circos-based tool to visualize genome assembly consistency or synteny between assemblies.
  ☆74Updated 2 months ago
• CenterForMedicalGeneticsGhent / PREFACE
  PREFACE -- PREdict FetAl ComponEnt
  ☆13Updated 3 years ago
• ARTbio / tools-artbio
  Collection of galaxy tools developed by the artbio-platform at the IBPS (Institut de Biologie Paris-Seine)
  ☆12Updated 2 months ago
• caballero / SeqComplex
  Algorithms to compute DNA complexity
  ☆34Updated 2 years ago
• nanoporetech / ont_tutorial_basicqc
  A bioinformatics tutorial demonstrating a best-practice workflow to review a flowcell's sequence_summary.txt
  ☆30Updated 4 years ago
• fritzsedlazeck / Spectre
  Copy number caller for long read data including SNV utilization
  ☆55Updated 4 months ago
• ggonnella / gfaviz
  Graphical interactive tool for the visualization of sequence graphs in GFA format.
  ☆67Updated 6 years ago
• ChaissonLab / danbing-tk
  Toolkit for VNTR genotyping and repeat-pan genome graph construction
  ☆24Updated 2 weeks ago
• MatteoSchiavinato / all2vcf
  Toolkit to convert the output of common variant calling programs to VCF
  ☆21Updated 2 years ago