Computer simulation of genetic mechanism !!
...ype Data for Pedigree Structures http://bioinformatics.org/simped/ Simprot A program to simulate protein evolution by substitution, insertion and deletion http://www.uhnre...2958 days ago
BBTools for bioinformatician !
...rate is the number indicating substitution, insertion, or deletion (X, I, D). Ex...tations. You can specify the number of snps, insertions, deletions, and Ns per read,...tations. You can specify the number of snps, insertions, deletions, and Ns per read,...2254 days ago
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Genome Assembly Tools and Software - PART2 !!
...the string graph. MindTheGap 1.0.0 – Detection and Assembly of Insertion VariantsMindTheGap is a software that performs detection and assembly of DNA insertion variants in NGS read datasets...2669 days ago
Useful Publications and Websites for Deep Sequencing Data Analysis
...ge Genome-wide LORE1 retrotransposon mutagenesis and high-throughput insertion detection in Lotus japonicus....ing to allow use of Illumina sequencing to screen for retrotransposon insertion mutations, and includes a sof...3762 days ago
List of generic simulation software/tools/resource with brief description and homepage !!!
...Genotype Data for Pedigree Structures http://www.hgsc.bcm.tmc.edu/content/simpedSimprot A program to simulate protein evolution by substitution, insertion and deletion http://www.uhnre...3720 days ago
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Dr. Ken Buetow: IS & Personalized Medicine Lecture-Part 1
...ciently and accurately computationally identify variants. More recently, the analytic approaches have been extended to systematically identify insertion/deletion variation, transloca...3853 days ago
3787 days ago
Perl script to insert the DNA string in genome
...my $file = $ARGV[0]; # input fasta file (genome file) my $out = $ARGV[1]; # output fasta file my $chr="test"; #insertion chromosome my $pos=10; # position of the insertion my $seqI = "AAAA"; #sequence...2642 days ago
Insert the sequence at desire location in multi-fasta file with Perl
#!/usr/bin/perl use warnings; use strict; use Bio::SeqIO; use Bio::Seq; use File::Copy; #ARGV[0] should be in following format --- Keep the coordinate sorted b...2297 days ago
NovelSeq: Novel Sequence Insertion Detection
The NovelSeq framework is designed to detect novel sequence insertions using high throughput paired-end whole genome sequencing data. http://novelseq.sourceforge.net/Home Paper at https://www.ncbi.nlm.nih.gov/pubmed/20385726Tags: NovelSeq, Novel, Sequence, Insertion, Detection
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Comment on "LAMSA: fast split read alignment with long approximate matches"
...NT] Mismatch penalty for SW-alignment. [3] -O --open-pen [INT(,INT,INT,INT)] Gap open penalty for SW-alignment(end2end-global: insertion, deletion, one-end-extend: insertion, deletion). [5(,5,5,5)] -E --...2106 days ago