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Exeter-Led Study Maps What an Average Human Genome Looks Like
A new study from the University of Exeter has characterized what counts as an “average” human genome, offering a reference point for normal genetic... -
Decoding the Genomics of Neurodegeneration with Large-Scale Long-Read Sequencing
Much of the genetic basis of Alzheimer's disease and related dementias (AD/ADRD) is still unexplained, and some of the answers may sit...Last edited by SEQadmin2; 10-01-2026, 06:03 AM. -
Chemotherapy Leaves Detectable DNA Signatures in Childhood Tumors
A study led by The Hospital for Sick Children (SickKids), published in Nature, found that nearly half of childhood tumors treated with common chemotherapies... -
The Application of Whole Genome Sequencing (WGS) in Agricultural Breeding
Whole genome sequencing (WGS) has revolutionized the field of genetic breeding by enabling breeders to identify and select desirable genetic traits in...Last edited by Novogene; 11-01-2024, 10:16 AM. -
Exploring the Power of Whole Genome Sequencing: A Beginner’s Guide to Long-read Sequencing
In recent years, whole genome sequencing (WGS) has revolutionized the field of genetics and opened up new avenues for scientific exploration. It allows...
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Whole Genome Sequencing (WGS) Service for Cancer
Whole genome sequencing (WGS) is a key driver for many medical research projects in cancer and complex genetic disorders. Creative Biolabs has established... -
Whole Genome Sequencing (WGS) Service for Cancer
Whole genome sequencing (WGS) is a key driver for many medical research projects in cancer and complex genetic disorders. Creative Biolabs has established... -
Webinar: Build High-Quality Genome Assemblies of Small Organisms with HiFi Sequencing
Did you know that you can generate highly accurate long reads from only a few nanograms of input DNA? Find out how at our next webinar on July 8.
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RNASeq & Whole Genome(DNA) Seq Analysis Training in Mumbai, India
WHAT: 2-day Technical Training in NGS Data Analysis | Whole Genome (DNA) Sequencing & RNASeq in Mumbai, India
WHEN: 6-7 March 2020... -
Any user friendly way to find rare mutations in whole genome raw?
Is there any user friendly way to find rare mutations in the individual human whole genome sequencing raw data? (from Dante, 30x coverage).
...Last edited by Larendy; 01-07-2020, 03:38 PM. -
Gave the Wrong Indexes for WGS... but I know them!
I recently sent off 100+ genomes to be whole genome sequenced and I sent the incorrect ones for a couple... but I have the correct ones! Is there a method... -
Single index adapters for low-plex
Hi,
I'm very new to sequencing so apologies if my question is naive.
I am trying to sequence whole human genome samples... -
What are the best tools/practices for CNV detection/analysis?
I am looking for the current state-of-the-art tools/practices for CNV (structural variation) detection/analysis for family (trio) data produced by Illumina.... -
Sequence bacterial genome and amplicons on the same run
Hello everyone,
At the moment we are using Miseq to sequence both bacterial and viral genomes at very low throughput. I would like to know... -
Searching for specific sequences in WGS data
Hi everyone.
I have never worked with WGS data and have a question. I have several thousands of sequences that I can convert in any format...
