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Uncovering the Genetic Basis of Rare and Complex Diseases through Whole Genome Sequencing (WGS)
As the cost of sequencing decreases and more efficient sequencing technologies are developed, high-throughput sequencing methods are powerful tools for...
Last edited by Novogene; 08-13-2024, 07:15 AM. -
WGS vs WES: Which Genetic Sequencing Method is Right for You?
Whole genome sequencing (WGS) and whole exome sequencing (WES) are two of the most popular methods used in modern genetic research. While both methods...
Last edited by Novogene; 06-21-2024, 12:43 PM. -
What happens when a bioinformatician has his own genome sequenced for $300?
Of Course! He goes even deeper by analyzing the analysis itself!
Unveil the mysteries of genetics as a bioinformatician explores his own... -
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... -
Assemble Anaeroplasma species genome from whole genome sequencing
Hi everyone,
I have a fasta file containing reads generated by PacBio whole genome sequencing of a feces sample from mouse. I need to extract... -
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... -
calling SNVs in shallow WGS data from liquid biopsy
Hi All,
could there be any reasonably reliable SNV calling approach in the following scenario: I have shallow (1-3x) WGS sequencing data... -
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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Annovar Annotation for CanFam3
Dear community members,
I am currently trying my luck with the tool called ANNOVAR in my attempt to filter out my huge data of SNP called... -
Determining quality of genome assembly
Hi! I apologize for this really basic question, as I am new to the field.
I am looking for homologous genes in various species using BLAST.... -
Question: Not-Merged Reads What to do?
Hey guys,
So I'm working with pair-end data and I'm concerning regarding the merged/not-merged reads. I'm currently merging them using PEAR and... -
Lists of somatic mutations from WGS
Dear all,
I am looking for lists of somatic mutations from cohorts of patient (>=50 patients).
There are some discussions about...Last edited by Jane M; 05-02-2019, 07:51 AM. -
diagnostics labs - what do they use?
Hi all, just wondering what the current state-of-play is with regards to clinical diagnostics labs, whether in the UK, European, or US context. Are small... -
very low coverage WGS on Novaseq 6000?
Is it possible to multiplex more than 384 samples on a Novaseq 6000 in order to obtain very low coverage WGS (0.5-2x)? -
Has anyone used Pathoscope pipeline for wgs?
Tool link here: https://sourceforge.net/p/pathoscope/wiki/Home/
I'm trying to process some WGS fastq files. I'm not clear on on the process...
