bioinformatics

This partnership is poised to revolutionize clinical insights and decision-making for the pharma industry with the aim of enhancing therapeutic efficacy and commercial lifespan.

Gene Ontology is an expanding knowledgebase that provides scientists with universal definitions to describe the functions of genes and their products. 

In this webinar, Austin Holmes and Jason Koth will discuss how to overcome single cell methylation and data analysis hurdles.

Calculating the polygenic risk scores of ancient humans such as Ötzi the iceman helps researchers understand the genetic predisposition to cardiovascular disease.

An open-source search engine helps scientists identify hundreds of microbial metabolites in a matter of seconds. 

Comprehensive genome sequencing of 13,880 tumors revealed somatic and germline mutations that could influence patient treatment and prognosis.

In this webinar, Joshua Campbell will talk about the fundamentals of scRNA-seq analysis and how to handle various challenges. 

Centralized core facilities and commercial service providers specializing in NGS provide expertise and training for researchers new to the method.

Researchers show how a toxic therapy helped identify a mummy using preserved DNA.

Tumors contain thousands of genetic changes, but only a few are actually cancer-causing. A quicker way to identify these driver mutations could lead to more targeted cancer treatments.

In this webinar, an expert panel will discuss nucleic acid recovery and sequencing methods from biological samples found in unusual habitats.

In this webinar, Sarkis Mazmanian and Daniel Mucida highlight how intestinal bacteria influence neuronal function and regeneration.

Rafael Gomez-Amaro and Karen Ersland discuss how HyperFinder technology optimizes cell identification and isolation from flow cytometry assays.

Researchers seek genomic clues to understand differences in the immune response to infection.

Melissa Vos discusses how lipids’ good intentions become harmful in Parkinson’s Disease.

Timothy O’Sullivan and Jacob Blum will discuss how they use single cell data to understand complex biological systems.

Aleksei Aksimentiev and Stefan Howorka discuss challenges in amino acid sensing with nanopores and approaches to design efficient protein sequencing technology.

A look at how ancient events crafted modern human DNA and their potential impact on human health.

Researchers sample and sequence bacteria from biological and environmental sources to learn how to overcome selective pressure