Using UNIX

Using Perun

RAM and CPU memory - Perun Queues

Perun and Environments

GitHub repositories of the lab

Other software locations

Databases locations

BLAST+ and v5 database user guide

BLAST and PLAST

Taxonomy recovery from BLAST/PLAST output

Making Bioconda recipes

The idea of this section is to share command line tips and tricks that you have found made it a lot easier to do bioinformatics work. This can range from basic UNIX things like setting up your terminal environment, configuring your SSH connections or managing your filesystem to explaining new bioinformatics tools and how to work with large scale computer clusters.

Recordings of the Tips and Tricks meetings are available for downloading or viewing online here

Setting up your terminal environment

Command line hotkeys

ls expanded

wc expanded

head and tail expanded

sort expanded

uniq expanded

cut expanded

cat expanded

nohup

grep expanded

awk for tabulated files

SSH Keys

Passwords and Passphrases

The SSH Config

Viewing tabular BLAST outfiles

Viewing alignment files

Handy custom functions

Manipulating FASTA FILES

RNA-Seq Processing

[Short reads] Cleaning of Illumina Paired-end reads

[Short reads] Short read assembly

[Short reads] depth and breadth of coverage

[Long reads] MINION Sequencing from START to FINISH

[Long reads] Assembling Long Read Data

[Long reads] Nanopore tools for polishing

Decontamination using a metagenomics approach (Anvi’o)

Decontamination using read classifier (Eukfinder)

Decontaminating reads using DECONSEQ

[Genome] Binning tools

[Genome] Evaluating genome completeness using Benchmarking Universal Single-Copy Orthologs (BUSCO)

[Genome] Evaluating genome quality using CGAL

[Mito genome] Using Mitoprot

[Mito genome] Visualizing mitochondrial genomes

Changing contig or scaffold names in a genome assembly

Extracting a single fasta entry (or multiple) from a multifasta file

Getting protein or CDS sequences from a gff file

de novo transcriptome assembly with Trinity

de novo transcriptome assembly with rnaSPAdes

[RNA-seq reads] Mapping RNAseq data to your genome

[Transcriptome] Evaluating and comparing transcriptome assemblies with rnaQUAST

[Transcriptome] TransDecoder for transcriptomes

Differential gene expression analysis

Gene prediction with just GeneMark

Gene prediction with just Augustus

Gene prediction with Braker2 pipeline

Gene prediction with the Funannotate pipeline

Improving gene models with fix_genes_with_false_introns.py

Gene prediction curation with IGV

From Nanopore to Gene Prediction

Functional annotation with the Funannotate pipeline

Finding genes of interest with PANTHER HMMs

Search Protocol for Orthologs of Components of Key molecular systems (SPOCK)...\\ SORRY this is not up and running yet. Please complain with Dayana!

Orthologs searches using panther HMMRs

Dayana Salas - Utility scripts(taxonomy, coloring trees, phylogenetics, mixture models, domain architecture and more)

[Phylogeny] Multi-gene phylogeny pipeline

Distinguishing LGT from contaminants

Running RevBayes with multiple cores

Curation of phylogenomic datasets

Ploidy analysis using ploidyNGS

Python Resources

[Q&A] Real cases of bash/shell scripts「Ongoing」

Q&A others

Do Bioinformaticians have naming regrets?

A little of what you fancy does you good!

Playground

Who looks after which page