Full Length Plasmid Sequencing Service
abm’s Plasmid Sequencing service utilizes the power of next generation sequencing for plasmid verification (obtaining the full length sequence of any plasmid). Unexpected mutations and wrong sequence information can affect downstream applications and lead to unnecessary troubleshooting slowing down your research progress. With as little as 1 ng of plasmid DNA, the plasmid sequencing service can provide comprehensive full length coverage for any plasmid, something that has only recently become achievable. A maximum plasmid size of 50kb is included with this service; larger plasmids can be accommodated for an additional fee.
abm is an Illumina Certified Service Provider, dedicated to ensuring the delivery of the highest-quality data available for genetic analysis applications.
"Thanks for being so responsive to our feedback and the quick turnaround on the re-assembly. That is great customer service! I'll be sure to pass along our positive experience to my colleagues."Dr. Bryce Kerlin, Center for Clinical & Translational Research at Nationwide Children's Research Institute, Full-Length Plasmid Sequencing/NGS
"I am a fan of abm: great product quality, great price, great rewards and great experience."Dr. Vincent Emond, Centre de recherche du CHU de Québec CHUL
|Paired-end sequencing||UNIT||CAT. NO.||Unit Price|
|Full Length Plasmid Sequencing (100 Mb, 2x150bp PE)||1 Sample||IW10001||$315.00|
|SERVICE NAME||UNIT||CAT. NO.||UNIT PRICE|
|de novo Genome Assembly & Plasmid Annotation||1 Sample||IB00022||$60.00|
|Gap closure by Sanger sequencing (per Gap)||1 Gap||IB00024||$99.00|
|SERVICE NAME||UNIT||CAT. NO.||UNIT PRICE|
|DNA Isolation for NGS||1 Sample||IW19001||$60.00|
|Sample and Library QC||1 Sample||IR18001||$60.00|
|Data Storage (per additional 3 months)||IS10001||$150.00|
|Hard Drive of NGS Results||1 Hard Drive||IS10003||Inquire|
Key Features for abm's Full Length Plasmid Sequencing Service
|Starting Material||1-50ng of plasmidDNA|
|Sequencing Type||2 x 150bp PE|
|Bioinformatics Analyses||De novo assembly
Gap Closure by Sanger sequencing
|Turn-around Time||About 4-6 weeks from passing sample QC|
|Data Storage||3 months|
Project Design/Advice Assistance
Confidentiality and Service Policy
Our goal is always to deliver high-quality useful data to aid you in your research. We perform extensive maintenance and quality assurance on our equipment and strict quality control of samples throughout the sequencing process. However, next-generation sequencing by nature does not always deliver equally robust results due to a variety of factors, such as the variability inherent in the library preparation process, the biochemistry that takes place during sequencing and the quality of samples that we receive. We will make every effort to deliver the number of reads that are listed, although it is not possible to guarantee that those targets will always be achieved. The actual number of reads passing filter may vary by up to 10% from the listed target. Studies by various institutes have shown that there is minimal difference in coverage for 10% variation in reads past 5-10 million total reads.
All services are for research use only.
|Is your company certified as a service provider for Illumina Sequencing?|
Yes, we are a certified Illumina service provider.
|What kind of analysis software do you use for sequence analysis?|
The Illumina sequencers come with the integrated software that can perform the regular bioinformatics analysis functions. In addition, we have extensive experience with other open access software such as Galaxy, Adnuril, BioBike, etc. In other words, we are willing to perform additional bioinformatics analysis with different software and tools to satisfy a variety of demands from our customers.
|What kind of QC methods do you adopt for the customer's sample(s)?|
We will perform QC on your Total RNA samples prior to sequencing them, using the Agilent Bioanalyzer (industry standard) to determine the RNA Integrity Number (RIN). If the RIN is lower than 8, we consider these samples as having failed QC. If the samples do not pass QC, we will ask you to send us new samples. If we do not receive new samples, thereby cancelling the sequencing order, there will be a QC fee of $50/sample. This fee will be waived if you choose to continue with the sequencing order. A strict positive and negative control will be applied to this QC process. The library QC will also be performed using the Agilent Bioanalyzer to determine library size and purity. Also, prior to loading the libraries on the sequencer, we perform qPCR quantification. The cost for this is included in the sequencing service. For the QC of the final data from our sequencing service, the integrated software will generally do the job and provide adequate QC information, however, we can also provide additional QC data such as FASTQC upon request. The data we output will pass our Q30 filter, which means that the error rate in base calls is less than 1 in 1000, or 0.1%. We will get a percentage at the end of the run which states the percentage of bases that have a Q score > 30, and this percentage is usually ≥85%.
|What is the lead time for your WGS, WES, and RNA-Seq services?|
Our sequencing lead times depend on workload, but are typically 2-4 weeks for sequencing data + 2-3 weeks for standard analysis. Please inquire for lead times for more detailed analysis.
|01||Barclay, R. A. et al. "Exosomes from uninfected cells activate transcription of latent HIV-1." J. Biol. Chem 292(28):11682-11701 (2017). DOI: 10.1074/jbc.A117.793521. Application: RNA-Seq.|
|02||Ee, LS et al. "An Embryonic Stem Cell-Specific NuRD Complex Functions through Interaction with WDR5." Stem Cell Rep 8(6):1488-1496 (2017). DOI: 10.1016/j.stemcr.2017.04.020. Application: RNA-Seq.|
|03||Acharya, D et al. "KAT-Independent Gene Regulation by Tip60 Promotes ESC Self-Renewal but Not Pluripotency." Cell Rep 19(4):671-679 (2017). DOI: 10.1016/j.celrep.2017.04.001 .Application: RNA-Seq.|
|04||Goudarzi, R et al. "Effects of Arthrocen, an avocado/soy unsaponifiables agent, on inflammatory mediators and gene expression in human chondrocytes." FEBS Open Bio 7(2):187-194 (2017). DOI: 10.1002/2211-5463.12176. Application: RNA-Seq.|
|05||Taylor, J.F. et al. "In Vitro Effects of Arthrocen, an Avocado/Soy Unsaponifiables Agent, on Inflammation and Global Gene expression in Human Monocytes." IJC 9(4):31-39 (2017). DOI: 10.5539/ijc.v9n4p31. Application: RNA-Seq.|
|06||Alam, S.B. and Rochon, D. "Cucumber Necrosis Virus Recruits Cellular Heat Shock Protein 70 Homologs at Several Stages of Infection." J Virol 90 (7):3302-3317 (2016). DOI: 10.1128/JVI.02833-15. PubMed: 26719261. Application: RNA-Seq.|
|07||Ghoshala, K et al. "Encapsidation of Host RNAs by Cucumber Necrosis Virus Coat Protein during both Agroinfiltration and Infection." J Virol 89(21):10748-61 (2015). DOI: 10.1128/JVI.01466-15. PubMed: 26269190. Application: Next Generation Sequencing.|
|08||Nakamura, S et al. "Novel roles for LIX1L in promoting cancer cell proliferation through ROS1-mediated LIX1L phosphorylation." Sci Rep 5:13474: (2015). DOI: 10.1038/srep13474. PubMed: 26310847. Application: Next Generation Sequencing.|