SIMulator for Long read transcriptome Analysis with RNA DecaY model
-
Updated
Aug 10, 2020 - Python
SIMulator for Long read transcriptome Analysis with RNA DecaY model
Analyses of Penter, Borji & Nagler et al., 2023
Suite of tools for use in genome assembly and consensus. Work in progress.
Long read structural variants in rare disease cohort
A web-documentary about uranium mining in Mongolia and it's consequences for the nomads, living there.
A safe place for the personal scripts used in the long-read benchmarking project.
tool for long read transcriptome assembly
Performs archiving and transfer of Nanopore sequencing data
Fast and space-efficient taxonomic classification of long reads
Analyse RNA feature distributions.
preqclr is a software tool that reports on quality for long read sequencing data without the use of a reference genome.
Merge transcriptome read-to-genome alignments into non-redundant transcript models
MuSTA: Multi-Sample Transcriptome Assembly for long-read isoform sequencing
Sensitive and Fast Alignment Search Tool for Long Read sequencing Data.
Demultiplexing and debarcoding tool designed for LR-Split-seq data.
Minor Variant Calling and Phasing Tools
BELLA: a Computationally-Efficient and Highly-Accurate Long-Read to Long-Read Aligner and Overlapper
Toolkit for calling structural variants using short or long reads
A Python library to visualize and analyze long-read transcriptomes
Add a description, image, and links to the long-read topic page so that developers can more easily learn about it.
To associate your repository with the long-read topic, visit your repo's landing page and select "manage topics."