Targeted sequencing is an effective way to sequence and analyze specific genomic regions of interest. This method enables researchers to focus their efforts on their desired targets, as opposed to other methods like whole genome sequencing that involve the sequencing of total DNA. Utilizing targeted sequencing is an attractive option for many researchers because it is often faster, more cost-effective, and only generates applicable data. While there are many approaches to targeted...
16 results in 0.0022 seconds.
-
Targeted Sequencing: Choosing Between Hybridization Capture and Amplicon Sequencing
Targeted sequencing is an effective way to sequence and analyze specific genomic regions of interest. This method enables researchers to focus their efforts on their desired targets, as opposed to other methods like whole genome sequencing that involve the sequencing of total DNA. Utilizing targeted sequencing is an attractive option for many researchers because it is often faster, more cost-effective, and only generates applicable data. While there are many approaches to targeted...Last edited by seqadmin; 12-15-2025, 10:24 AM. -
SeqCap EZ HyperCap Workflow for Target Enrichment
Does anyone have experience with SeqCap EZ HyperCap Workflow for Target Enrichment protocol from Roche? I'm unable to find any public datasets I can look... -
Custom Panels for Targeted Sequencing
We offer MYbaits® as a complete system for efficient, in-solution target enrichment for high-throughput sequencing. The MYbaits family of products provides... -
reggiardo.anselmo started a topic Low Coverage using target enrichment on Ion Torrentin Ion TorrentLow Coverage using target enrichment on Ion Torrent
Hi everybody.
Hope you can help troubleshooting this issue.
I used to carry our BRCA1/BRCA2 target enrichment using Ampliseq paneles. However,... -
High capacity, low cost, targeted NGS
Hello SEQanswers
My name is Kurt Lamour and I run a company (Floodlight Genomics) that provides a new low cost option for targeted genetic sequencing... -
ForeignMan started a topic Handling duplicates and other biases in Haloplex enriched targeted sequencing datain GeneralHandling duplicates and other biases in Haloplex enriched targeted sequencing data
Hello everyone,
we're starting to work with deep sequencing data of target regions that were enriched by Agilent's Haloplex kit (Illumina... -
eSeminar: Genomic Research Panels Overview and Demo
Upcoming eSeminar
Genomic Research Panels Overview and Demo: How to Customize the HaloPlex Cancer Research Panel
Register Today... -
MYbaits target enrichment
Does anyone have any experience with MYcroarray's target enrichment kit (MYbaits). The cost of the kit is significantly lower than Illumina/Agilent kits... -
FFPE and Target Enrichment: A Match or a Mismatch?
Date and time: Thursday, September 20, 2012 8:00
Pacific Daylight Time
Program: Genomics eSeminar Series
Panelist(s) Info: Maria... -
Roche NimbleGen number of bases
I have 5 samples that were sequenced with SeqCap EZ Human Exome Library v2.0 kit from Roche/NimbleGen. I ran it with BWA for alignment and converted to... -
Calculating number of reads per target base
Hi,
I have results of whole exome NGS (SureSelect, enrichment by hybridization) as fastq files and I want to get the the list of target sequences... -
Webinar: Revolutionize Your Desktop Sequencing Workflow with HaloPlex
Revolutionize Your Desktop Sequencing Workflow with HaloPlex.
April 4, 2012
Presenter: Sheila Purim, Ph.D., Product Manager, Agilent Technologies,... -
Efficient targeted resequencing of human germline and cancer genomes by oligonucleoti
Hi everyone, check out our new sequence capture method, recently published in NBT. We are calling the method oligonucleotide-selective sequencing (OS-Seq)....Last edited by JBuenrostro; 10-26-2011, 09:30 PM. -
Questions on Agilent SureSelect Indexing Kit
Hi,
does anybody have details on the new SureSelect Indexing Kits?
I am interested in targeting 12 samples and pool and sequence them... -
Problems with recent Illumina multiplexing
In October 2009, I prepared a paired-end multiplexed genomic DNA library using Illumina's kits and enriched for my regions of interest using Agilent's...
