vojtechruz / pyladies-7Links
Repository with code examples and homework for the 7th run of Pyladies CZ Praha
☆49Updated 2 weeks ago
Alternatives and similar repositories for pyladies-7
Users that are interested in pyladies-7 are comparing it to the libraries listed below
Sorting:
- Website of the Czech PyLadies chapter / Web českých PyLadies☆45Updated this week
- Website with learning materials / Stránka s učebními materiály☆324Updated 3 weeks ago
- Materiály pro lekce pokročilého Pythonu pro PyLadies Ostrava☆9Updated 5 years ago
- A deep learning method for sgRNA off-target propensity prediction.☆14Updated 5 years ago
- TideHunter: efficient and sensitive tandem repeat detection from noisy long reads using seed-and-chain☆20Updated last year
- PacBio BAM C++ library☆21Updated last year
- ☆16Updated 2 years ago
- Graph-based mapping of long sequences, noisy or HiFi.☆55Updated 4 years ago
- Example client programs for Saphetor's VarSome annotation API☆33Updated 4 months ago
- Big Browser watching your genome☆11Updated 9 years ago
- Optimized Dynamic Genome/Graph Implementation: understanding pangenome graphs☆213Updated last month
- simple viewer for variant call format using htslib☆32Updated 8 years ago
- Using de-novo assembly and read-phasing to assemble reference-free diploid genomes☆22Updated last week
- Biopet docs☆17Updated 6 years ago
- new repo☆28Updated 4 years ago
- Testing module for Galaxy workflows☆10Updated 6 years ago
- MNase-seq analysis pipeline using BWA and DANPOS2.☆11Updated last year
- PBSIM2: a simulator for long read sequencers with a novel generative model of quality scores☆72Updated last year
- Documentation for PEP specification and all PEPkit software☆9Updated last month
- Toolkit for VNTR genotyping and repeat-pan genome graph construction☆26Updated last week
- Reference-free duplex sequencing pipeline.☆18Updated 2 years ago
- create a gemini-compatible database from a VCF☆56Updated 4 years ago
- Galaxy tools and workflows developed at the Earlham Institute☆14Updated 2 months ago
- Tool to annotate outfiles from ExpansionHunter and TRGT with the pathologic implications of the repeat☆32Updated last week
- A tool to extract LOH blocks from VCF, BAM and FASTA data☆23Updated 9 months ago
- ☆36Updated 7 years ago
- Copy number caller for long read data including SNV utilization☆65Updated 2 months ago
- A Scalable GPU-Based Whole Genome Aligner, published in SC20: https://doi.ieeecomputersociety.org/10.1109/SC41405.2020.00043☆72Updated 10 months ago
- ☆12Updated 6 years ago
- A sequence demultiplexer for the Illumina HiSeq technology☆21Updated 12 years ago