Structural variation: the hidden genomic treasure
...s (SVs) such as deletions, insertions, duplications, inversions and translocations litter genomes and are often...uctural variation includes balanced variants such as inversions and translocations, and unbalanced ones such as...2694 days ago
Chromosome breakpoint - a breakup to remember
...chniques can also help identify the exact location of the breakpoint and the nature of the rearrangement, such as translocations, inversions, deletions, or duplications. Translocations are one of the most common ty...416 days ago
2685 days ago
simuG: a general-purpose genome simulator
...simulating the full-spectrum of genomic variants (single nucleotide polymorphisms, Insertions/Deletions, copy number variants, inversions and translocations) for any organisms (including...1611 days ago
Genome Assembly Tools and Software - PART1 !!
...nbsp;tex directory). The assembly does not only encode SNPs and short INDELs, but also retains long deletions, novel sequence insertions, translocations and copy numbers REPdeno...2677 days ago
Breaking chromosomes to study cancer !!!
...ocal translocation. Reciprocal chromosomal translocations occur following double-strand...growth and survival pathways, such as the translocations seen in leukemia and childhoo...it is possible to obtain such chromosomal translocations. The CRISPR-Cas9 system is ex...3570 days ago
Dr. Ken Buetow: IS & Personalized Medicine Lecture-Part 1
...onally identify variants. More recently, the analytic approaches have been extended to systematically identify insertion/deletion variation, translocations, and rearrangements. In appl...3862 days ago
Create random 2 translocations in genome !
...ed: 1925195826 The option translocation_count has been specified: translocation_count = 2 [Sun Jan 10 17:12:58 2021] Introducing random Translocations based on the following parame...1202 days ago
Structural variation: the hidden genomic treasure
Genome re-sequencing projects have revealed substantial amounts of genetic variation between individuals extending beyond single nucleotide polymorphisms (SNPs) and short indels. Structural Variations (SVs) and Copy Number Variations (CNVs) are a major source of genomic variation. However, compar...Tags: Bioinformatics, Chromosome, Genome, NGS, Structure Variation, Deletions, Insertions, Duplications, Inversions, Translocations
2694 days ago
407 days ago