Results for "Genome Interpretation"
Top-level pages
Reformat is a member of the BBMap/BBTools package. It is a multipurpose tool designed for converting reads or oth...flag "-Xmx2g". For example, to change the line-wrapping length on the human genome (which...2762 days ago
List of Bioinformatics Software Tools for Next Generation Sequencing
...Seq, ChIP-Seq, Small RNA-Seq, Genome Browser, visualizations, Biological Interpretation, etc. Supports workfl...SnpEff Input: BAM Reference Genome: FASTA indexed with SAMtools faidx O...Splicing Enhancer; useful for interpretation of point mutations/polymorphi...2957 days ago
Tools for Searching Repeats And Palindromic Sequences
What are genomic interspersed repeats? In the mid 1960's scientists discovered that many genomes contain stretches of highly repetitive...ve been copied to another region of the genome.Interspersed RepeatsProcessed...s which have been reintegrated into the genome with th...2260 days ago
- alignment: the mapping of a raw sequence read to a location within a reference genome. The mapping occurs because t...equence read to the reference genome. Three core abbreviations are...c variants. RNAME: reference genome identifier (also known as the...e sequence Referencesequence/genome ...
2918 days ago
Genome Assembly Tools and Software - PART1 !!
...reported for the assembly of genomes while the others are designed aiming at handling complex genomes. TriMetAss 1.2 – Th.... It can also facilitate data interpretation and hypothesis genera...Phusion 2.1c – Assembly Genome Sequences from Whole Genome Shotgun(W...2734 days ago
Quick next generation sequencing (NGS) terms definition
fragment size: the Illumina WGS protocol generates paired-end reads from both end...concordant if they can be mapped to the reference genome as “expected”: (a...p;a read that can only be mapped to the reference genome by brea...2571 days ago
Alignment-free sequence comparison tools available for next-generation sequencing data analysis
kallisto Transcript abundance quantification from RNA-seq d...https://github.com/bioinfo-ut/GenomeTester4/ Phy-Mer Reference-i...SNPs (dbSNP and Affymetrix's Genome-Wide Human SNP Array) from ra...., ONT or PacBio reads, draft genomes) Software (Perl) https://g...2420 days ago
- When you have both Illumina and Nanopore data, then SPAdes remains a good option for hybrid assembly - SPAdes was...des.py will show you the options: spades.py This produces: SPAdes genome assembl...
2400 days ago
Single Cell RNAseq data analysis tutorial !!
A major breakthrough (replaced microarrays) in the late 00’s and has been widely used since Measures the...and reveal cell-type-specific expression changes in type 2 diabetes http://genome.cshlp.o...2399 days ago
Tools for bacterial whole genome annotation
RAST – Web tool (upload contigs), uses the subsyst...ation (if you have only a few genomes to annotate). Prokka &...y useful if you have loads of genomes or need to annotate a pangen..., as well as other functional genome units such as structural RNAs...2380 days ago
