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DAVIS SEQUENCING, INC. Company Profile

23:38 EDT 17th June 2018 | BioPortfolio

We offer DNA sequencing of single stranded or double stranded DNA samples from purified plasmids and PCR products. Our sequencing reactions are performed using the Applied Biosystems Big Dye Terminator V3.0 sequencing chemistry. One sequencing reaction consists of one DNA template (customer supplied plasmid DNA or PCR product) being sequenced with one primer (customer supplied primer or one of our supplied primers). We supply several frequently used sequencing primers for free, but the template DNA samples are supplied by our customers.
Our sequencing reaction read-lengths are normally between 800 and 900 bases (with a basecalling accuracy >99%) when run on our ABI 3730 DNA sequencers. Sequencing read-lengths are dependent upon several factors including template DNA concentration, purity and base composition (poly A and/or T regions, GC content and short tandem repeats) as well as primer binding specificity.

Since DNA sample purity and concentration are the two most critical factors to the success of automated sequencing reactions, we highly recommend that customers use the QIAGEN® plasmid DNA prep kits to purify their plasmid DNA samples. For purifying PCR products, we recommend using either the QIAquick Gel Extraction Kit (supplied by QIAGEN®) or Centricon® 100 columns (supplied by Amicon®) to remove unincorporated dNTPs and primers. In our experience, other DNA purification kits and methods are less reliable for preparing automated sequencing quality DNA samples. Please call us if you have any questions regarding the compatibility of other DNA sample preparation methods with our DNA sequencers.

Location

1490 Drew Avenue, Suite 170
Davis
California
95616
United States of America

Contact

Phone: (530) 297-5038
Fax: (530) 297-5039
Email: info@davissequencing.com


News Articles [466 Associated News Articles listed on BioPortfolio]

UC Davis researchers discover how antiepileptic drugs induce birth defects

(University of California - Davis Health System) UC Davis School of Medicine researchers identify mechanism by which a common drug for treating epileptic seizures can lead to birth defects if used dur...

UC Davis researchers find new way to defeat HIV latency

(University of California - Davis Health System) Researchers at UC Davis Health, together with colleagues at UC San Francisco and the University of North Carolina at Chapel Hill, have found a mechanis...

How Media Portrayal Affects Women, And What Geena Davis Is Doing About It

Through the Geena Davis Institute on Gender in Media and the #StrengthHasNoGender campaign, Davis aims to change the portrayal of women in television shows, movies, and advertising, which in turn may ...

How Media Portrayal Affects Women And What Geena Davis Is Doing About It

Through the Geena Davis Institute on Gender in Media and the #StrengthHasNoGender campaign, Davis aims to change the portrayal of women in television shows, movies, and advertising, which in turn may ...

Whole Genome Sequencing of Babies

(Nuffield Council on Bioethics) – Whole genome sequencing of babies explores the ethical issues raised by whole genome sequencing of babies. Whole genome sequencing is cheaper and faster than ev...

Transformative technology

(University of California - Davis Health System) UC Davis neuroscientists have developed fluorescence sensors that are opening a new era for the optical recording of dopamine activity in the living br...

Illumina Launches iSeq 100 Sequencing System

Industry-Leading Sequencing Technology for Under $20K SAN DIEGO–(BUSINESS WIRE)–Illumina, Inc. (NASDAQ: ILMN) announced today the launch of the iSeq™ 100 Sequencing System. The new,...

Mike Davis Looks at the Past, the Present, and the Future of EHR Adoption—and Customization

Mark HaglandMike Davis, perhaps best known as one as a co-creator of the EMRAM schematic, which measures EHR implementation advancement, in his work at KLAS Research, is working to advance EHR develop...

PubMed Articles [745 Associated PubMed Articles listed on BioPortfolio]

Untitled by Ann Davis.

2017 Elda E. Anderson Award - Jason Davis.

Response to Davis and Behm (doi: 10.1089/jpm.2017.0608): Discontinuation of Statins.

Assessment of the cPAS-based BGISEQ-500 platform for metagenomic sequencing.

More extensive use of metagenomic shotgun sequencing in microbiome research relies on the development of high-throughput, cost-effective sequencing. Here we present a comprehensive evaluation of the p...

HLA Typing from Short-Read Sequencing Data with OptiType.

The established standards for HLA genotyping rely on targeted DNA sequencing techniques. However, the increasing abundance of short-read sequencing data has prompted a demand for computational tools c...

Clinical Trials [403 Associated Clinical Trials listed on BioPortfolio]

Bioequivalence Study of Gabapentin 800 mg Tablets Under Fed Conditions

This study compared the relative bioavailability (rate and extent of absorption) of Gabapentin tablets 800 mg by Ranbaxy Laboratories Limited with that of Neurontin ® 800 mg tablets of Pa...

Enabling Personalized Medicine Through Exome Sequencing in the U.S. Air Force

The MilSeq Project is a nonrandomized, prospective pilot study of whole exome sequencing (WES) in the U.S. Air Force. The purpose of this study is to explore the implementation of WES into...

Rapid Whole Genome Sequencing Study

Rapid Whole Genome Sequencing (rWGS) has proven to provide much faster diagnoses than traditional clinical testing, including clinical Whole Exome Sequencing (WES) and standard Whole Genom...

Bioequivalence Study of Gabapentin 800 mg Tablets Under Fasting Conditions

This study compared the relative bioavailability (rate and extent of absorption) of the test Gabapentin tablets 800 mg by Ranbaxy Laboratories Limited to the reference Neurontin ® 800 mg ...

Genomic Sequencing in Patients With HCM Undergoing Septal Myectomy

Investigators aim to use comparative exome and/or genome sequencing to discover causative molecular lesions for phenotypes hypothesized to be caused by somatic mutations. For this study, i...

Companies [244 Associated Companies listed on BioPortfolio]

Nucleics Pty Ltd

Nucleics was founded in 1999 by Dr Paul March and Dr Daniel Tillett to develop the ASIN genome sequencing technology. Nucleics is focused on the development of automated DNA sequencing services, reage...

Davis Vision

Headquartered in Plainview, N.Y., Davis Vision is one of America's leading vision benefits companies, providing comprehensive vision benefits for nearly 50 years. More than 55 million individuals nati...

Davis Phinney Foundation

The Davis Phinney Foundation was created in 2004 by cycling legend Davis Phinney. Davis Phinney remains the race leader in victories by an American cyclist, and he is a two-time Tour de France stage w...

DAVIS SEQUENCING, INC.

We offer DNA sequencing of single stranded or double stranded DNA samples from purified plasmids and PCR products. Our sequencing reactions are performed using the Applied Biosystems Big Dye Terminato...

Davis Vision, Inc.

Davis Vision is part of the HVHC Inc. group of companies, which also includes Viva International Group and Eye Care Centers of America. One of the nation's premier managed vision care companies, Davis...

More Information about "DAVIS SEQUENCING, INC." on BioPortfolio

We have published hundreds of DAVIS SEQUENCING, INC. news stories on BioPortfolio along with dozens of DAVIS SEQUENCING, INC. Clinical Trials and PubMed Articles about DAVIS SEQUENCING, INC. for you to read. In addition to the medical data, news and clinical trials, BioPortfolio also has a large collection of DAVIS SEQUENCING, INC. Companies in our database. You can also find out about relevant DAVIS SEQUENCING, INC. Drugs and Medications on this site too.

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DNA sequencing
DNA sequencing is the process of determining the precise order of nucleotides within a DNA molecule. During DNA sequencing, the bases of a small fragment of DNA are sequentially identified from signals emitted as each fragment is re-synthesized from a ...

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