Privatre:bioinfomatics

Bioinfomatics

A combined technologies with biology, computer science, mathmatics and statistics.

Bioinfomatics workflow steps

1. quality control assessmemt steps
2. sequence alignment
3. data summarization into genes/regions
4. data annotation to genomics features
5. statistical comparisons
6. mutltiomic ingetration

Bioinfomatics curated software list

• Package suites
• Data Tools
  • Downloading
  • Compressing
• Data Processing
  • Command Line Utilities
• Next Generation Sequencing
  • Workflow Managers
  • Pipelines
  • Sequence Processing
  • Data Analysis
  • Sequence Alignment
    • Pairwise
    • Multiple Sequence Alignment
    • Clustering
  • Quantification
  • Variant Calling
    • Structural variant callers
  • BAM File Utilities
  • VCF File Utilities
  • GFF BED File Utilities
  • Variant Simulation
  • Variant Prediction/Annotation
  • Python Modules
    • Data
    • Tools
  • Assembly
  • Annotation
• Long-read sequencing
  • Long-read Assembly
• Visualization
  • Genome Browsers / Gene Diagrams
  • Circos Related
• Database Access
• Resources
  • Becoming a Bioinformatician
  • Bioinformatics on GitHub
  • Sequencing
  • RNA-Seq
  • ChIP-Seq
  • YouTube Channels and Playlists
  • Blogs
  • Miscellaneous

• Online networking groups

File format in Bioinfomatics

This section explains some of the commonly used file formats in bioinformatics

File formats	File extensions
FASTA	.fa, .fasta, .fsa
FASTQ	.fastq, .sanfastq, .fq
SAM (Sequence Alignment Map)	file.sam
BAM	file.bam
VCF (Variant Calling Format/File)	file.vcf
GFF (General Feature Format or Gene Finding Format)	file.gff2, file. gff3, file.gff
GTF (Gene Transfer format)	file.gtf

Usufull Tutorial Link

• https://vcru.wisc.edu/simonlab/bioinformatics/programs/
• https://github.com/danielecook/Awesome-Bioinformatics
• https://mybiosoftware.com/
• https://bioinformatics.uconn.edu/resources-and-events/tutorials-2/
• Cluster system software modules - https://bioinformatics.uconn.edu/cbc_software/software-2/

We can use BIOConda

Bioconda only supports python 2.7, 3.6, 3.7, 3.8 and 3.9 -> DLS38 can be used

Lib and sources

Libraries	Mamba or manual	Description	References
meme	Mamba
BWA	Mamba	BWA is a software package for mapping low-divergent sequences against a large reference genome, such as the human genome. It consists of three algorithms: BWA-backtrack, BWA-SW and BWA-MEM.	https://bio-bwa.sourceforge.net/ https://wikis.utexas.edu/display/bioiteam/BWA
samtools	Mamba
ncbi-blast+	Manual	ScalaBLAST is a high-performance multiprocessor implementation of the NCBI BLAST library. ScalaBLAST supports all 5 primary program types (blastn, blastp, tblastn, tblastx, and blastx) and several output formats (pairwise, tabular, or XML).	https://blast.ncbi.nlm.nih.gov/doc/blast-help/downloadblastdata.html https://vcru.wisc.edu/simonlab/bioinformatics/programs/install/blastplus.htm https://ftp.ncbi.nlm.nih.gov/blast/executables/blast+/
somatic-sniper	Mamba	a software for comparing tumor and normal pairs. The developer estimate its sensitivity and precision, and present several common sources of error resulting in miscalls.
breakdancer	Mamba	a  package that provides genome-wide detection of structural variants from next generation paired-end sequencing reads
tigra-sv	Manual	a program that conducts targeted local assembly of structural variants (SV) using the iterative graph routing assembly (TIGRA) algorithm (L. Chen, unpublished). It takes as input a list of putative SV calls and a set of bam files that contain reads mapped to a reference genome such as NCBI	https://bioinformatics.mdanderson.org/public-software/archive/tigra/
TopHat		Please note that TopHat has entered a low maintenance, low support stage as it is now largely superseded by HISAT2 which provides the same core functionality	Not support Python 3
HISAT2	Mamba	HISAT2 is a fast and sensitive alignment program for mapping next-generation sequencing reads (both DNA and RNA) to a population of human genomes as well as to a single reference genome.
cufflinks	Manual	manual install to prefix (231216) hpcmate@223vmbase:~/biolib/download/cufflinks-2.2.1.Linux_x86_64$ ls -al	https://github.com/cole-trapnell-lab/cufflinks
bedtools	Mamba
T-COFFEE	Mamba
mafft	Mamba
maq	Manual	Maq stands for Mapping and Assembly with Quality It builds assembly by mapping short reads to reference sequences. hpcmate@223vmbase:~/biolib/compile/maq/maq-0.7.1$	https://maq.sourceforge.net/maq-man.shtml https://mybiosoftware.com/sim4-20030613-align-expressed-dna-sequence-genomic-sequence.html https://mybiosoftware.com/maq-0-7-1-mapping-assembly-qualities.html Why do you need MAQ? Its latest version is more than 10 years old - I think you would be better of using some newer program. MAQ is really old, and by now it has problems compiling with current compilers. You can use the fpermissive flag to get it to compile: make CFLAGS="-Wall -m64 -D_FASTMAP -DMAQ_LONGREADS -g -O2 -fpermissive" CXXFLAGS="-Wall -m64 -D_FASTMAP -DMAQ_LONGREADS -g -O2 -fpermissive" Note I took the CFLAGS and CXXFLAGS from the Makefile, and appended -fpermissive to them. Your CFLAGS and CXXFLAGS may be different, check them before issuing make. Three executables, `maq', `maq.pl' and `farm-run.pl', will be copied to /usr/local/bin by default.
muscle,	Mamba
phyml	Mamba
, primer3,	Mamba
probcons,	Mamba
sim4,	Manual	(231216) hpcmate@223vmbase:~/biolib/compile/sim4/sim4.2012-10-10$ or	https://globin.bx.psu.edu/ftp/dist/sim4/https://globin.bx.psu.edu/html/docs/sim4.html
tigr-glimmer	mamba	tigr-glimmer
amap-align	???
dialign -> dialign2	mamba
emboss	mamba
exonerate	mamba
kalign2 & kalign3	mamba
CNVnator	mamba
CREST	mamba
CAP3	mamba
Cluster -> mmseqs2	mamba
Cluster	mamba
FastQC	mamba
fastx_toolkit	mamba
IGVTools	mamba
MACS -> macs2	mamba	Need Python < 3
Meerkat -> django-meerkat	pip	pip install django-meerkat
RNAcode
RNAz
RepeatMasker
SNVMix2
SOAPdenovo2-src
VarScan
ViennaRNA
bismark
blat
circos
clustalw
clustalx
cnD
cpc
fasta
gmap-gsnap
lobstr
meme
, , , , , , , , ,, , , , , , , , , , , miRDP, mirdeep2, picard-tools, polyphen, rseq, seqtk-master, sickle-master, snpEff, soap
rSeq: RNA-Seq Analyzer		https://jhui2014.github.io/rseq/	On 61 sever, /test/bioinfomatics/rseq/rseq-0.2.2-src
SNVMix2		https://github.com/shahcompbio/snvmix	imp@CGX-GPU:~/test/bioinfomatics/snvmix (master)$
Samtools		SAM (Sequence Alignment/Map) format is a generic format for storing large nucleotide sequence alignments	https://samtools.sourceforge.net/ https://sourceforge.net/projects/samtools/files/samtools/ https://github.com/samtools/samtools/blob/develop/INSTALL
Breakdancer		BreakDancer uses CMake which is a cross-platform build tool. Basically it will generate a Makefile so you can use make. The requirements are the zlib, development library, gcc, gmake, cmake 2.8+. Beginning with version 1.4.4, BreakDancer includes samtools as part of the build process # --recursive option is important so that it gets the submodules too $ git clone --recursive https://github.com/genome/breakdancer.git	https://github.com/genome/breakdancer/tree/master https://breakdancer.sourceforge.net/https://vcru.wisc.edu/simonlab/bioinformatics/programs/install/breakdancer.htm https://github.com/shendurelab/LACHESIS/issues/30