Day: December 9, 2020
AVIA 3.0: Interactive Portal for Genomic Variant and Sample Level Analysis
Motivation: The Annotation, Visualization and Impression Evaluation (AVIA) is an online utility combining a number of options to annotate and visualize genomic variant information. Customers can examine practical significance of their genetic alterations throughout samples, genes, and pathways. Model 3.Zero of AVIA presents filtering choices by way of interactive charts and by linking illness related information sources. Newly […]
First report of Berkeleyomyces basicola causing mango root rot and decline in India
Mango wilt has been a severe constraint in mango (Mangifera indica L.) manufacturing in a number of nations together with India (Shukla et al. 2018). Though, a number of fungal pathogens have been reported related to the illness, species of Ceratocystis, Verticillium and Lasiodiplodia have been discovered predominantly chargeable for the wilt (Shukla et al. […]
CRISPR/Cas genome editing to optimize pharmacologically active plant natural products
Since time immemorial, human use medicinal vegetation as sources of meals, remedy and industrial goal. Classical biotechnology and up to date next-generation sequencing (NGS) strategies have been efficiently used to optimize plant-derived natural-products of biomedical significance. Earlier, protein based mostly enhancing instruments viz. zinc-finger nucleases (ZFNs) and transcription activator-like endonucleases (TALENs) have been popularized for […]
Comprehensive genomic analysis of microenvironment phenotypes in ovarian cancer
Background: Ovarian most cancers is without doubt one of the main causes of cancer-related loss of life in girls. The incidence of ovarian most cancers is insidious, and the recurrence fee is excessive. The survival fee of ovarian most cancers has not considerably improved over the previous decade. Just lately, immune checkpoint inhibitors equivalent to these […]
A Collaborative Effort to Define Classification Criteria for ATM Variants in Hereditary Cancer Patients
Background: Gene panel testing by large parallel sequencing has elevated the diagnostic yield but in addition the variety of variants of unsure significance. Scientific interpretation of genomic information requires experience for every gene and illness. Heterozygous ATM pathogenic variants improve the danger of most cancers, notably breast most cancers. For that reason, ATM is included in most hereditary […]
Improving interpretation of genetic testing for hereditary hemorrhagic, thrombotic, and platelet disorders
The final 10 years have seen an explosion within the quantity of knowledge out there by next-generation sequencing. These knowledge are advancing rapidly, and this tempo makes it tough for many practitioners to simply sustain with all the new info. Complicating this understanding is usually conflicting details about variant pathogenicity and even in regards to […]