Protocol for De novo Genome Assembly using Illumina Reads
...genomics/ingap and http://ingap.sourceforge.net/inGAP is also useful for finding structural variants between genomes from read mappings. Genome finishing tools:Semi-automated gap fill...1205 days ago
2543 days ago
MIX: Combining multiple assemblies from NGS data
...nes two or more draft assemblies, without relying on a reference genome and has the goal to reduce contig fragmentation and thus speed-up genome finishing. The proposed algorithm build...2190 days ago
Genome Assembly Tools and Software - PART2 !!
...st 12 years to get assembly jobs done efficiently – and especially accurately. That is, without actually putting too much manual work into finishing the assembly. HapCompass 0.7...2687 days ago
Genome Assembly Tools and Software - PART1 !!
...ysis to diagnose, report, and automatically improve de novo genome assemblies. Phred/Phrap/Consed 29.0 – DNA Sequence Assembler & Finishing Tools phrap is a program f...2687 days ago
Install Python locally on shared Linux server !
...wing command to install pip as a local user wget --no-check-certificate https://bootstrap.pypa.io/get-pip.py -O - | python - --user #After finishing the installation, we need to...2099 days ago
Tags: Finishing, NGS, Scaffoldings
2543 days ago
Tags: Consed, Finishing, Package, BAM, Viewer, Assembly, Editor, Autofinish, Autoreport, Autoedit, Align, Reads, Reference, Sequence
1550 days ago