
GitHub - dellytools/delly: DELLY2: Structural variant discovery by ...
Delly is an integrated structural variant (SV) prediction method that can discover, genotype and visualize deletions, tandem duplications, inversions and translocations at single-nucleotide resolution in short-read and long-read massively parallel sequencing data.
《Delly:结构变异检测的强大工具》 - GitCode博客
2025年1月18日 · Delly是一款强大的开源工具,能够高效地发现、分型和可视化短读段和长读段测序数据中的缺失、串联重复、倒位和易位等结构变异。 本文将详细介绍Delly的安装与使用方法。
delly安装和使用 | 生物信息文件夹
2022年7月20日 · delly 是一款结构变异 (SV) 预测软件,可以单个碱基的分辨率检测基因分型和可视化缺失、串联重复、倒位和易位等结构变异。它使用双端reads、split reads和reads深度来检测结构变异。
结构变异(SV)分析软件DELLY - 百家号
2024年12月27日 · 基因组结构性变异包括BigIndel、重复、倒位、易位等,常用短读长测序检测,DELLY是经典软件,需bam文件和参考基因组,可检测体细胞和胚系变异。 遗传变异通常分为两类:序列变异和结构变异。 基因组结构性变异(Structure Variantions,简称SVs)通常指基因组上大长度的序列变化和位置关系变化。 基因组结构性变异类型很多,包括长度在50bp以上的长片段序列插入或者删除(Big Indel)、串联重复(Tandem repeate)、染色体倒位(Inversion) …
delly/README.md at main · dellytools/delly · GitHub
Delly is an integrated structural variant (SV) prediction method that can discover, genotype and visualize deletions, tandem duplications, inversions and translocations at single-nucleotide resolution in short-read and long-read massively parallel sequencing data.
CNV calling | DELLY - 简书
Delly is an integrated structural variant (SV) prediction method that can discover, genotype and visualize deletions, tandem duplications, inversions and translocations at single-nucleotide resolution in short-read massively parallel sequencing data. It uses paired-ends, split-reads and read-depth to sensitively and accurately delineate genomic ...
Delly2 - Research Computing Documentation - University of …
2023年3月13日 · From the Delly2 Home Page: Delly2 is an integrated structural variant prediction method that can discover and genotype deletions, tandem duplications, inversions and translocations at single-nucleotide resolution in short-read massively parallel sequencing data.
How to speed up "delly call -g hg19.fa -v sites.bcf -o s1.geno
2021年6月1日 · I'm trying to run "delly call -g hg19.fa -v sites.bcf -o s1.geno.bcf -x hg19.excl s1.bam". When the sites.bcf is relatively small, say 7MB, and the size of s1.bam is 90GB, the process takes about 5 hours. However, when the size of the sites.bcf grows to 48MB (I merged more samples to get sites.bcf), the process takes about 52 hours.
Delly 鉴定SV - 简书
2021年7月18日 · git clone --recursive https://github.com/dellytools/delly.git cd delly/ make all 或者下载最新版本即可使用. wget https://github.com/dellytools/delly/releases/download/v0.8.7/delly_v0.8.7_linux_x86_64bit Delly同时支持多线程运算,只需在运行命令行前加 export OMP_NUM_THREADS=8, 线程数≤ 样本数. 2 …
Run Delly to get structural variants - Yuwei Bao's personal website
2023年4月21日 · Delly needs a sorted, indexed and duplicate marked bam file for every input sample.