wangkaisine / SGE-On-CentOS
Intro how to install and use SGE(Sun Grid Engine) on ConteOS 7
☆19Updated 6 years ago
Related projects ⓘ
Alternatives and complementary repositories for SGE-On-CentOS
- Easily submitting multiple PBS jobs or running local jobs in parallel. Multiple input files supported.☆28Updated last year
- ☆34Updated last year
- A pipeline for isoseq☆23Updated 6 years ago
- ☆14Updated 6 years ago
- HomBlocks: A multiple-alignment construction pipeline for organelle phylogenomics based on locally collinear block searching☆32Updated 7 years ago
- Plant small RNA target prediction tool☆25Updated 7 years ago
- Converting and demultiplexing of PacBio BAM files into gzipped fasta and fastq files.☆36Updated last year
- This python script can be used to detect Whole-genome duplication (WGD) with the dS based method.☆23Updated 5 years ago
- CNV Rapid Aberration Detection And Reporting☆11Updated 3 years ago
- Python scripts for matching output of Pacific Biosciences IsoSeq RNA-seq pipeline to an annotation file.☆24Updated 9 years ago
- Simultaneous multi-sample transcript assembler for RNA-seq data☆17Updated 2 years ago
- This is the Haplotypo repository☆20Updated 5 months ago
- modPhred is a pipeline for detection of DNA/RNA modifications from raw ONT data☆16Updated 6 months ago
- Scripts involved in our workflow for detecting CNVs from WGS data using read depth-based methods☆45Updated 2 years ago
- ☆14Updated 6 years ago
- Noise-Cancelling Repeat Finder☆24Updated last year
- ☆26Updated 10 months ago
- KOBAS: a command line tool for identifying significant pathways from genomic data☆30Updated 14 years ago
- genome basic statistics tool (e.g. n50, n10, ng50,...)☆14Updated 12 years ago
- A python package for the identification of lncRNA from the assembled novel transcripts☆17Updated 3 years ago
- SAMStat displays various properties of next-generation sequencing reads stored in SAM/BAM format.☆24Updated last year
- Awk, bash, python scripts for processing NGS data☆14Updated 9 years ago
- MapOptics is a lightweight cross-platform tool that enables the user to visualise and interact with the alignment of Bionano optical mapp…☆17Updated 2 years ago
- This is used to achieve haplotype-resolved assembly of tetraploid genomes using gamete sequencings☆11Updated 3 years ago
- a hidden Markov model to infer simple repeats from genome sequences☆34Updated 3 years ago
- This toolkit deals with GEnomic sequence and genome structure ANnotation files between inbreeding lines and species.☆45Updated last year
- Streamlined duo/trio analysis and pedigree haplotyping: from VCF to interactive HTML☆13Updated 3 weeks ago
- ☆16Updated 7 months ago
- TQSLE v1.0 released☆10Updated last year