BOL: Related items

The Genome 10K Project

Tue, 29 Jul 2014 09:11:04 -0500

https://genome10k.soe.ucsc.edu The Genome 10K project aims to assemble a genomic zoo—a collection of DNA sequences representing the genomes of 10,000 vertebrate species, approximately one for every vertebrate genus. The trajectory of cost reduction in DNA sequencing suggests that this project will be feasible within a few years. Capturing the genetic diversity of vertebrate species would create an unprecedented resource for the life sciences and for worldwide conservation efforts. The growing Genome 10K Community of Scientists (G10KCOS), made up of leading scientists representing major zoos, museums, research centers, and universities around the world, is dedicated to coordinating efforts in tissue specimen collection that will lay the groundwork for a large-scale sequencing and analysis project.

Assistant Professor - Genetics, Genomics, Evolution, and Development - Molecular & Cell Biology

Fri, 14 Aug 2026 09:54:00 -0500

Salary range: The current salary range for this position is $84,100 - $132,900 (9-month academic year salary), however, off-scale salary and other components of pay, which would yield compensation that is higher than this range, are offered to meet competitive conditions.
Anticipated start: July 1, 2027
Application Window
Open date: July 27, 2026
Next review date: Monday, Oct 19, 2026 at 11:59pm (Pacific Time)
Apply by this date to ensure full consideration by the committee.
Final date: Monday, Oct 19, 2026 at 11:59pm (Pacific Time)
Applications will continue to be accepted until this date.
The Department of Molecular and Cell Biology (MCB) at the University of California, Berkeley invites applications for a tenure-track faculty position in the Genetics, Genomics, Evolution, and Development (GGED) Division, at the Assistant Professor level.

More at https://evoldir.net/brian/evoldir/Jobs//UC-Berkeley.Tenure_track_faculty_in_genetics_genomics_evolution_and_development

Research Associate at Indian Institute of Chemical Technology (IICT), Hyderabad

Thu, 07 Aug 2014 01:55:21 -0500

Indian Institute of Chemical Technology (IICT), Hyderabad, a constituent of CSIR is a leading research Institute in the area of chemical sciences. The core strength of IICT lies in Organic Chemistry, and it continues to excel in this field for over six decades. The research efforts during these years have resulted in the development of several innovative processes for a variety of products necessary for human welfare such as drugs, agrochemicals, food, organic intermediates, adhesives etc. More than 150 technologies developed by IICT are now in commercial production.

CSIR-IICT is conducting Walk in Interview for the following position on a purely temporary basis for the sponsored project "GENESIS (BSC-0121) at 10.00 AM on 19th August 2014 at IICT, Hyderabad

Position : Research Associate
No of Post : One
Desired Profile : PhD in computation biology or M.Tech in Computational Biology with three years experience in relevant subject and atleast one research paper in SCI journal

Experience : Knowledge in vector and vector borne disease, disease modeling, GIS mapping and modeling.
Age : 35 years
Stipend : Rs 22000/- + HRA

Eligible candidate may download the application form from our website http://www.iictindia.org and appear for interview along with the duly filled in application form supported by bio-data and one set of attested photo copies of certificates of educational qualification, age, experience, caste, latest photograph and the cadndidates are required to bring all the original certificates for verification

Walk in Interview : 19.08.14

AI Uncovers Hidden Secrets in Bacterial DNA, Opening New Frontiers in Genomic Research

Jitendra Narayan — Fri, 25 Sep 2026 22:38:42 -0500

Scientists are now using artificial intelligence in order to examine sections of bacterial DNA that have not been looked at before. This method is showing potential RNA interactions and previously unknown genetic systems which could alter our understanding of microbes. A new study presents Minerva, a genome language model, demonstrating that AI can assist researchers in identifying biological patterns that traditional techniques might fail to detect.

The study, which was made available as a preprint on bioRxiv on 23 September 2026, focuses on the non-coding sections of DNA that are still largely unknown. Although these areas do not produce proteins, they can contain important signals and instructions which have an effect on cell function. The research presents a novel approach to investigating how bacteria handle and control their genetic information.

AI maps previously unexplored genomic regions

The team developed Minerva in order to identify possible interactions between different regions in microbial genomes; rather than depending on similarities with known sequences, Minerva predicts these relationships directly from the DNA by using patterns learned by a genome language model.

On 150 bacterial genomes, Minerva identified a large number of interactions that were not included in the existing annotations. The researchers stated that 84.3 per cent of the predicted intergenic base-pairing interactions were not present in the current annotations, which demonstrates that AI can be of help in generating new ideas in biology.

Unusual RNA structures and viral genetic systems identified

The study also examined a bacterial RNA family known as TwoAYGGAY in Pseudomonas; the model anticipated longer RNA structures and identified associations with repeated DNA sequences, thus providing new insights into how these non-coding elements are organised and how they have evolved.

In a separate section of the study, the researchers examined reverse transcriptase systems associated with bacteriophages, which are viruses that infect bacteria. They identified RNA arrays that maintain their structure but have different sequences and were linked to Unknown Group 27 reverse transcriptases. The findings indicate that these RNAs could function as templates for the production of complementary DNA that is capable of forming hairpin shapes.

The researchers also observed that Minerva was able to detect patterns associated with protein-coding areas, even though it had not been trained to do so. This indicates that genome language models may pick up on biological signals that go beyond what they were intended to identify.

Implications for future genomic research

The fact that artificial intelligence is becoming increasingly important in the field of microbial genomics is shown by the fact that models such as Minerva are able to predict interactions and identify patterns in areas which have not been extensively studied, thus helping researchers to decide what to study next and enabling them to gain a better understanding of biological systems that are still not well understood.

Yet the predictions do not reveal the exact function of each element identified. In order to verify which of the predicted interactions actually take place in living cells and the way in which they affect the microbes, experiments will be necessary. Although the study has undergone peer review, it does nonetheless offer a promising illustration of how machine learning can complement traditional genomics and assist scientists in moving from the identification of known genes to the exploration of the complex relationships that shape microbial life.

More at https://www.biorxiv.org/content/10.64898/2026.09.22.753630v2.full.pdf

Webinar on 'An integrated RNA and DNA approach to unravel genetic regulation in cancer'

Yeshodari — Wed, 11 Feb 2015 04:59:57 -0600

Webinar on 'An integrated RNA and DNA approach to unravel genetic regulation in cancer'

Abstract

Whole exome DNA sequencing (WES) or whole genome DNA sequencing (WGS) allows detection of mutations and polymorphisms in all exonic and genomic regions, respectively, while messenger RNA sequencing (RNA-Seq) enables quantitative analysis of gene expression. Mutations in the genome result in diverse transcriptional aberrations that can be missed in a stand-alone WES/WGS analysis. An integration of DNA variant analysis and RNA-Seq analysis enables one to investigate the consequences of genomic changes in the RNA transcripts including germline and somatic changes, imprinting, RNA editing and allele specific expression (ASE). In this webinar, we will demonstrate this integrated approach using Strand NGS to identify high confidence mutations, RNA editing events and ASE in cancer.

Webinar Details

Sessions	San Francisco Time (PST)	Tokyo Time (GMT+09:00)	Berlin Time (GMT+01:00)	Mumbai Time (GMT+05:30)
Session 1	25 Feb 12:30 AM	25 Feb 5:30 PM	25 Feb 9:30 AM	25 Feb 2:00 PM
Session 2	25 Feb 9:00 AM	26 Feb 2:00 AM	25 Feb 6:00 PM	25 Feb 10:30 PM

Register here: http://www.strand-ngs.com/webinar_registration

About Speaker:

Dr. Veena Hedatale, has a PhD in Plant Genetics from The Radboud University, Netherlands focused on meiosis and recombination. Her prior academic experience at Cornell University was on genetic mapping and gene transformation in Rice. She has worked with Monsanto, and contributed to data mining, database development as well as gene/promoter/pathway discovery for traits related to yield and stress in crop species. At Strand, Veena has worked on Pharmacogenomic analysis of targets and Gene family analysis projects. Currently, she is part of the Strand NGS Application Science team and is involved in the analysis of next generation sequencing data.

Please feel free to contact us 24/5, for availing free online training or if you have any questions.

Email: sales@strandngs.com

Phone (USA): 1-800-752-9122

Phone (ROW): +1-650-353-5060

kraken: A universal genomic coordinate translator for comparative genomics

Jit — Thu, 07 Dec 2017 04:45:43 -0600

If you planning on conducting a study involving dozens of large genomes, then you do not have to run all pairwise synteny alignments .. simply try kraken: A universal genomic coordinate translator for comparative genomics

Address of the bookmark: https://github.com/nedaz/kraken

Biology, Computers Collide in High-Demand Field of Bioinformatics

Mon, 25 Aug 2014 00:56:10 -0500

Dr. Shivas Amin calls bioinformatics a "collision of biology and computers." Students learn how to use computers and skills in math and biology to analyze genome and proteome projects to prepare for high-demand jobs in the life sciences. Learn more about Amin and hear from student Medina Baitemirova and alumnus Lukas Simon about the fast-growing field of bioinformatics.

Scribl : HTML5 canvas genomics graphic library

Jit — Thu, 25 Oct 2018 09:38:53 -0500

Scribl is a javascript, Canvas-based graphics library that easily generates biological visuals of genomic regions, alignments, and assembly data. Scribl can also be used in conventional offline pipelines, since everything needed to generate charts can be contained in a single html file.

Address of the bookmark: http://chmille4.github.io/Scribl/

A comprehensive atlas of human gene activity released !!!

Abhimanyu Singh — Tue, 02 Sep 2014 14:20:24 -0500

A large international consortium of researchers has produced the first comprehensive, detailed map of the way genes work across the major cells and tissues of the human body. The findings describe the complex networks that govern gene activity, and the new information could play a crucial role in identifying the genes involved with disease.

We are able to pinpoint the regions of the genome that can be active in a disease and in normal activity, whether it’s in a brain cell, the skin, in blood stem cells or in hair follicles. This is a major advance that will greatly increase our ability to understand the causes of disease across the body.

The research is outlined in a series of papers published March 27, 2014, two in the journal Nature and 16 in other scholarly journals. The work is the result of years of concerted effort among 250 experts from more than 20 countries as part of FANTOM 5 (Functional Annotation of the Mammalian Genome). The FANTOM project, led by the Japanese institution RIKEN, is aimed at building a complete library of human genes.

Researchers studied human and mouse cells using a new technology called Cap Analysis of Gene Expression (CAGE), developed at RIKEN, to discover how 95% of all human genes are switched on and off. These “switches” — called “promoters” and “enhancers” — are the regions of DNA that manage gene activity. The researchers mapped the activity of 180,000 promoters and 44,000 enhancers across a wide range of human cell types and tissues and, in most cases, found they were linked with specific cell types.

Referene : www.kurzweilai.net/first-comprehensive-atlas-of-human-gene-activity-released

phyloXML: XML for evolutionary biology and comparative genomics

Jit — Sun, 08 Dec 2019 09:41:18 -0600

phyloXML (example) is an XML language designed to describe phylogenetic trees (or networks) and associated data. PhyloXML provides elements for commonly used features, such as taxonomic information, gene names and identifiers, branch lengths, support values, and gene duplication and speciation events. Using these standardized elements allows interoperability between various applications and databases. Furthermore, both due to extensible nature of XML itself and the provision of elements by phyloXML, extensibility as well as domain specific applications are ensured. The structure of phyloXML is described by XML Schema Definition (XSD) language.

http://www.phyloxml.org/archaeopteryx-js/adh.html

Address of the bookmark: http://www.phyloxml.org/