Next Generation Sequencing

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Exploring Mitochondrial DNA Mutations with Mosaicism in Cancer and Aging
ByNeermita Bhattacharya November 10, 2024October 22, 2026

Currently, we know that genomic variations are gathered up in somatic cells as one age, but we have a limited understanding of mitochondrial DNA (mtDNA) mosaicism. mtDNA has many effects on various diseases, particularly cancer, and they might have a role in the aging process. Unlike nuclear DNA, which is inherited from both parents, mtDNA…

Read More Exploring Mitochondrial DNA Mutations with Mosaicism in Cancer and Aging
AI | Bioinformatics | Genomics | Medical Informatics | News | Precision Medicine | Trending

Dante’s GenomeChat: Your Gateway to Personalized Genomic Insights
ByAnshika Gupta July 2, 2024October 22, 2026

Dante Genomics launched Dante GenomeChat, which enables users to receive highly personalized genomic information thanks to advanced technology. A graphical iOS app can access this new platform; it levels complex genetic data for each individual and translates it into something understandable and actionable. Dante GenomeChat is built on the foundation of Dante Genomics clinical genomics…

Read More Dante’s GenomeChat: Your Gateway to Personalized Genomic Insights
Bioinformatics | Genomics | News | NGS | Paper Summary | Transcriptomics | Trending

Choosing the Best Tool for Identifying Transcriptional Regulators: Navigating the NGS Landscape
ByAnchal Negi February 12, 2024October 22, 2026

This article delves into a recent study undertaken by a team of researchers that examined multiple computer algorithms for transcriptional regulator prediction using Next-Generation Sequencing (NGS) data. Grasping biological processes and developing personalized medications necessitates a deep understanding of gene control. Transcriptional regulators (TRs) control the expression of certain genes, and NGS technology has enabled…

Read More Choosing the Best Tool for Identifying Transcriptional Regulators: Navigating the NGS Landscape
AI | Big Data | Bioinformatics | Genomics | News | Paper Summary | Tools | Trending

Breaking Barriers in Genomic Research: DRAGEN Delivers Accurate Variant Detection in 30 Minutes
ByAnchal Negi January 7, 2024January 7, 2024

Scientists took decades to decode the complex code of DNA, and though we have come a long way, the journey is far from over. The development of DRAGEN sheds light on new unknown secrets, unlocking a deeper understanding of our bodies and nature around us. Illumina has always provided us with the best tools and resources, acting…

Read More Breaking Barriers in Genomic Research: DRAGEN Delivers Accurate Variant Detection in 30 Minutes
Bioinformatics | Corona Virus | COVID-19 | Covid-19 News | Genomics | News | NGS | Paper Summary | Sequencing | Trending

Scientists Devised a Bioinformatics Method ‘COJAC’ for Early Detection and Surveillance of SARS-CoV-2 Genomic Variants in Wastewater
ByTanveen Kaur July 21, 2022November 11, 2022

Using read pairs with several SARS-CoV-2 variant-specific signature mutations as a reliable signal of low-frequency variants, scientists develop the bioinformatics technique known as COJAC (Co-Occurrence adjusted Analysis and Calling). The genomic sequencing, in conjunction with COJAC, can offer population-level estimates of the prevalence and fitness of emerging variants from wastewater samples earlier and on the basis…

Read More Scientists Devised a Bioinformatics Method ‘COJAC’ for Early Detection and Surveillance of SARS-CoV-2 Genomic Variants in Wastewater
Bioinformatics | Cancer Research | News | NGS | Sequencing | Trending

NT-seq – A New Sequencing Technique for Genome-Wide Mapping of Different Types of DNA Methylation
ByDr. Tamanna Anwar July 3, 2022July 3, 2022

Baylor College of Medicine researchers introduce a new sequencing technique ‘NT-seq’ for simultaneously mapping all three forms of DNA methylation. All known methylation motifs in Escherichia coli and Helicobacter pylori genomes were reliably detected by NT-seq, which may also be utilized to find de novo methylation motifs. NT-seq offers a quick and effective way for genome-wide mapping of different…

Read More NT-seq – A New Sequencing Technique for Genome-Wide Mapping of Different Types of DNA Methylation
Bioinformatics | Cancer Research | News | NGS | Paper Summary | Precision Medicine | Trending

PGDx Elio Tissue Complete – An Automated and FDA-Approved Clinical Genomics Assay for Comprehensive Genomic Profiling of Human Cancer
ByTanveen Kaur May 30, 2022November 9, 2022

PGDx Elio tissue complete, which the FDA has approved for the analysis of 505 cancer-related genes, will enable the development of more effective precision oncology treatment options. The researchers from Personal Genome Diagnostics Inc. (PGDx) explain the developmental and analytical validation processes of the PGDx elio tissue complete test. It is an automated NGS-based approach…

Read More PGDx Elio Tissue Complete – An Automated and FDA-Approved Clinical Genomics Assay for Comprehensive Genomic Profiling of Human Cancer

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