wangkaisine / SGE-On-CentOSLinks
Intro how to install and use SGE(Sun Grid Engine) on ConteOS 7
☆19Updated 7 years ago
Alternatives and similar repositories for SGE-On-CentOS
Users that are interested in SGE-On-CentOS are comparing it to the libraries listed below
Sorting:
- Easily submitting multiple PBS jobs or running local jobs in parallel. Multiple input files supported.☆29Updated 2 years ago
- ☆39Updated 2 years ago
- Noise-Cancelling Repeat Finder☆26Updated 2 years ago
- Python scripts for matching output of Pacific Biosciences IsoSeq RNA-seq pipeline to an annotation file.☆23Updated 10 years ago
- barcode demultiplexing☆21Updated 6 years ago
- Nanopore basecalling and consensus decoding☆46Updated 3 years ago
- Structural variant merging tool☆57Updated last year
- a hidden Markov model to infer simple repeats from genome sequences☆36Updated 4 years ago
- Scripts involved in our workflow for detecting CNVs from WGS data using read depth-based methods☆46Updated 3 years ago
- Command line tools for CMDB varaints browser☆23Updated last year
- ☆14Updated 7 years ago
- Comprehensive benchmark of structural variant callers☆48Updated 4 years ago
- Generate unique KMERs for every contig in a FASTA file☆48Updated 3 years ago
- Nanopore raw signal repeat detection pipeline☆45Updated 2 years ago
- fastx-utils using klib☆20Updated 5 years ago
- wgs_pipeline☆18Updated 12 years ago
- Long-read Isoform Quantification and Analysis☆38Updated 8 months ago
- Official code repository for JAX-CNV☆14Updated 5 years ago
- An accurate repeat detection from Nanopore data using deep learning and image techniques☆24Updated 2 years ago
- A simple tool to calculate reads number and total base count in FASTQ file☆21Updated 6 years ago
- Streamlined duo/trio analysis and pedigree haplotyping: from VCF to interactive HTML☆15Updated last year
- A tutorial on structural variant calling for short read sequencing data☆38Updated last year
- wg-blimp: an end-to-end analysis pipeline for whole genome bisulfite sequencing data☆28Updated 3 years ago
- Genotyping of segregating mobile elements insertions☆19Updated 4 years ago
- Accurate Typing of Human Leukocyte Antigen (HLA) by Oxford Nanopore Sequencing☆17Updated 7 years ago
- Specifications for PacBio® native file formats☆31Updated last year
- HiFi-SR is a Python-based pipeline for the detection of plant mitochondrial structural rearrangements based on the mapping of PacBio high…☆10Updated 8 months ago
- microRNA PREdiction From small RNA-seq data☆30Updated 7 years ago
- Computes various SV statistics☆14Updated 2 years ago
- A tool for genotyping Variable Number Tandem Repeats (VNTR) from sequence data☆47Updated last year