biocorecrg / MOP2Links
Master of Pores 2
☆23Updated 9 months ago
Alternatives and similar repositories for MOP2
Users that are interested in MOP2 are comparing it to the libraries listed below
Sorting:
- POSTRE: Prediction Of STRuctural variant Effects☆28Updated 6 months ago
- Automated Detection and Qualification of Differential Methylation☆14Updated last year
- An R package for estimating poly(A)-tail lengths in Oxford Nanopore RNA and DNA reads.☆54Updated 11 months ago
- Long-read splice alignment with high accuracy☆63Updated 11 months ago
- for visual evaluation of read support for structural variation☆54Updated last year
- The Zavolab Automated RNA-seq Pipeline☆35Updated last month
- Splice junction analysis and filtering from BAM files☆42Updated 3 years ago
- Signal based nanopore RNA demultiplexing with convolutional neural networks☆38Updated last year
- perSVade: personalized Structural Variation detection☆40Updated last week
- modPhred is a pipeline for detection of DNA/RNA modifications from raw ONT data☆16Updated last year
- Immuological gene typing and annotation for genome assembly☆38Updated 6 months ago
- ✂️ Deep learning-based splice site predictor that improves spliced alignments☆54Updated 6 months ago
- ☆51Updated 6 years ago
- catalog for long-read sequencing tools☆32Updated 2 years ago
- A high throughput sequence read toolset using a streaming approach facilitated by Linux pipes☆50Updated 8 months ago
- ☆49Updated 10 months ago
- Structural variant caller☆55Updated 3 years ago
- Pipeline for de novo clustering of long transcriptomic reads☆26Updated 3 years ago
- A tutorial on structural variant calling for short read sequencing data☆39Updated 10 months ago
- Pipeline to evaluate and validate the accuracy of variant calling methods in genomic research☆35Updated this week
- detection of duplications and deletions using Python based machine learning techniques☆28Updated 6 years ago
- Structural variant merging tool☆54Updated last year
- Structural Variant Prediction Viewer☆35Updated 8 years ago
- Fully automated generation of UCSC assembly hubs☆34Updated 11 months ago
- ☆34Updated last year
- ☆33Updated 2 years ago
- Allo: a multi-mapped read rescue strategy for gene regulatory analyses☆24Updated last year
- Merge transcriptome read-to-genome alignments into non-redundant transcript models☆18Updated last year
- MetaSV: An accurate and integrative structural-variant caller for next generation sequencing☆58Updated 8 years ago
- Toolkit for the design and analysis of amplicon sequencing experiments utilizing unique molecular identifiers (UMIs)☆42Updated 3 weeks ago