Penn State (University Park) has both SOLiD and 454
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Sequencing Services provider
Ocimum Biosolutions,India :- Illumina/454/SOLiD/Informatics
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Just realized there's a duplication in the list. The Gene Pool is in University of Edinburg.Leave a comment:
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Updated! If you've used any of these services, please post your feedback in a new thread!Leave a comment:
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TCAG in Toronto, Canada offers NGS services for GAII, SOLiD 3 and 454 GS FLX
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FYI:
SOLID service provider in Taiwan - http://www.missionbio.com.tw/Leave a comment:
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Dear all,
this is a 454 sequencing service provider located in Italy, the english version of the web pages will be soon available.
BMR Genomics – Italy, Europe – 454 Titanium
[email protected]Leave a comment:
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Couple more...
I am based in Australia. Here are two more service providers from this region.
Geneworks - Illumina GA
Dept of Anatomy, University of Otago - Roche FLX and SOLiDLeave a comment:
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Yes, we take outside samples, unfortunately by law we have to charge 2x our internal pricing. Although, this is actually less than what most service companies are charging.
Our motivation is to increase the number of runs to reduce the service contract cost. Currently we have enough internal samples for 1 run a week. This leaves open a second run for external users.
If you have prepped libraries, there is essentially no wait for sequencing.Leave a comment:
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Sorry.. nevermind. Visited your site... it's clear from the webpage.Originally posted by doxologist View Post
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Developments in sequencing technologies and methodologies have transformed the field of epigenetics, giving researchers a better way to understand the complex world of gene regulation and heritable modifications. This article explores some of the diverse sequencing methods employed in the study of epigenetics, ranging from classic techniques to cutting-edge innovations while providing a brief overview of their processes, applications, and advances.
Methylation Detect...05-31-2023, 10:46 AM -
Differential Expression and Data Visualization: Recommended Tools for Next-Level Sequencing Analysis
After covering QC and alignment tools in the first segment and variant analysis and genome assembly in the second segment, we’re wrapping up with a discussion about tools for differential gene expression analysis and data visualization. In this article, we include recommendations from the following experts: Dr. Mark Ziemann, Senior Lecturer in Biotechnology and Bioinformatics, Deakin University; Dr. Medhat Mahmoud Postdoctoral Research Fellow at Baylor College of Medicine;...05-23-2023, 12:26 PM -
Continuing from our previous article, we share variant analysis and genome assembly tools recommended by our experts Dr. Medhat Mahmoud, Postdoctoral Research Fellow at Baylor College of Medicine, and Dr. Ming "Tommy" Tang, Director of Computational Biology at Immunitas and author of From Cell Line to Command Line.
Variant detection and analysis tools
Mahmoud classifies variant detection work into two main groups: short variants (<50...05-19-2023, 10:03 AM
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