yulab-ql / mhaESC_genome
☆11Updated 6 months ago
Alternatives and similar repositories for mhaESC_genome:
Users that are interested in mhaESC_genome are comparing it to the libraries listed below
- ☆18Updated 2 years ago
- ☆19Updated 9 months ago
- Enabling differential allele-specific analysis☆11Updated 4 months ago
- ☆24Updated 3 years ago
- ☆22Updated 4 months ago
- FINSURF is a tool designed to analyse lists of sequences variants in the human genome.☆12Updated 2 years ago
- DNA multiple sequence aligner, official version from Penn State's Miller Lab☆31Updated 6 years ago
- Identify and annotate TE-mediated insertions in long-read sequence data☆41Updated last year
- Immuological gene typing and annotation for genome assembly☆35Updated last month
- ☆17Updated 3 weeks ago
- ☆20Updated 6 months ago
- ☆16Updated 4 years ago
- Read level DNA methylation analysis of bisulfite converted sequencing data☆18Updated last year
- Summarise and plot data from long-read ONT (direct RNA/cDNA) BAM files☆14Updated last year
- Invertory of TE-gene isoforms☆10Updated last year
- A pipeline for identifying conserved topologically associating domain boundaries among multiple species.☆14Updated 9 months ago
- Hi-C Interaction Frequency Inference (HIFI): High-resolution estimation of DNA-DNA interaction frequency from Hi-C data☆23Updated 2 years ago
- Scripts and files used in the generation of the COLO829 somatic SV truthset.☆12Updated 3 years ago
- ☆35Updated 2 years ago
- ☆28Updated 4 months ago
- ☆22Updated last year
- ☆17Updated last year
- R package: TopDom - An efficient and Deterministic Method for identifying Topological Domains in Genomes☆21Updated last year
- Reproducibility workflow for Gigante et al., 2018: Using long-read sequencing to detect imprinted DNA methylation☆23Updated 6 years ago
- Jupyter Notebooks Using PGR-TK for various human pangenome analysis tasks☆15Updated 2 years ago
- A pipeline to detect chimeric transcripts derived from genes and transposable elements.☆26Updated last week
- ☆23Updated 3 years ago
- Clair3-RNA - a long-read small variant caller for RNA sequencing data☆22Updated last month
- A method for measuring chromosome-specific telomere length from long reads☆21Updated 11 months ago
- ☆9Updated 3 years ago