Neel
Bioinformatics Beginner
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The "Ifs" and "Buts" of NGS Quality Control and Trimming
By BioStar 429 days agoNGS quality control and trimming are essential steps to ensure reliable and accurate data for analysis. While the "ifs" highlight the clear benefits of these steps, the "buts" remind us of the potential pitfalls. By adopting best practices and...
My commonly used commands in Bioinformatics
Last updated 2781 days ago by Rahul NayakFYI, I've found it useful to use MUMmer to extract the specific changes that Racon makes, so I can evaluate them individually: minimap -t 24 assembly.fasta long_reads.fastq.gz | racon -t 24 long_reads.fastq.gz - assembly.fasta...Pacasus: Correction of palindromes in long reads from PacBio and Nanopore
By BioStar 2672 days agogithub.com - Tool for detecting and cleaning PacBio / Nanopore long reads after whole genome amplification. Check the poster from the Revolutionizing Next-Generation Sequencing (2nd edition) conference in the source...Shasta long read assembler
By Jit 2244 days ago Comments (1)github.com - The goal of the Shasta long read assembler is to rapidly produce accurate assembled sequence using as input DNA reads generated by Oxford Nanopore flow cells. Computational methods used by the Shasta assembler include: Using...mutatrix: a population genome simulator which generates simulated genomes.
By Jit 2230 days agogithub.com - genome simulation across a population with zeta-distributed allele frequency, snps, insertions, deletions, and multi-nucleotide polymorphisms More at https://github.com/ekg/mutatrix ./mutatrix -S sample -P test/ -p 2 -n 10 reference.fasta
Is reference genome necessary for gene expression study in transcriptome sequencing or for variant discovery in genome sequencing?
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