The ability to list and purchase bioinformatic analysis services along with next-gen sequencing comes to Genohub. This additional feature set will further simplify the NGS project experience by offering capabilities for the bioinformatics project step, all in one roof. By launching this service, researchers on Genohub are now able to shop from full-service sequencing providers who offer the three main services required in every NGS project with options for Illumina, Ion, SOLiD, PacBio, and Roche454 platforms:
- Library prep
- Next generation sequencing
- Bioinformatic analysis
The addition of this service alleviates the burden many researchers face of shopping for three separate sequencing related services from multiple providers and efficiently managing the entire process.
The benefits of this feature for researchers includes:
- Researchers save time and money purchasing sequencing and bioinformatic services simultaneously
- By enabling next gen sequencing providers to list bioinformatic services, it becomes easier and faster for researchers to compare and select a provider for their project
- Risk is mitigated, as researchers are able to purchase bioinformatic services along with NGS services by providers that have gone through the Genohub vetting process
Providers also benefit:
- Providers are now able to better highlight their unique services by listing specific bioinformatic services. These include basic primary analysis that may be included with every sequencing order, as well as more complex secondary and custom bioinformatics services that can be ordered as add-ons to NGS projects.
- The bioinformatics platform enables providers to more succinctly communicate bioinformatic services to researchers, cutting down on back and forth communication prior to the researcher opting to move forward with the services listed by the provider
Providers may now list bioinformatic analysis services on the familiar “Manage Services Offerings” page:
New Manage Services Page
Researchers will be able to view these services once they select to view details about a sequencing package found when shopping by project or technology.
At Genohub we constantly strive to improve the service we offer to the NGS community through the development of new features and functionality. When we launched Genohub in August, 2013 our goal was to launch a service that was useful to researchers and sequencing providers, and continue to enhance and improve our service based directly on feedback from our clients.
The bioinformatic analysis listing feature come as a direct result of our development methodology. Researchers asked for a one-stop-shop for all of their sequencing needs, and sequencing providers asked for more ways to highlight and differentiate their services on Genohub. You asked, we listened!
Please visit Genohub often as we are constantly adding new useful features to improve the next-gen sequencing shopping experience including upcoming features to further enable providers to differentiate themselves and mitigate risk in decision making for researchers. If you have any feedback on additional features you would like to see, please send us feedback by shooting us an email at firstname.lastname@example.org.
At Genohub, not only do we seek feedback from researchers, our development methodology is almost entirely based on this feedback. We receive this feedback via website forms as well as routine one-on-one conversations with some of the top researchers using next generation sequencing for their projects. Through this data and interaction, certain trends have begun to emerge which may be useful to an NGS provider seeking additional projects. This list is not based on a controlled experiment, however countless conversations indicate that these factors are extremely important:
- Turnaround time – this one is a toss up when compared with price, but we typically find turnaround time to be among the leading factors in a researcher’s decision to select an NGS provider. We have heard quite a few stories of researchers seeing turnaround times over several months for library prep and sequencing.
- Price – while this is one of the biggest factors for researchers, it must be qualified with established trust which is the next major factor.
- Trust – this one is a biggie for many researchers and often a non-starter if not established. The main reasons for this are that researchers are hesitant to ship their precious samples (ie human brain tissue) to an NGS provider for quite often costly sequencing if they are not confident in their abilities. Researchers have told us some of the things they look for which lend to building their confidence:
- Referrals & Reviews – researchers seek out colleagues who have done similar projects and look for recommendations. Word of mouth is one of the biggest methods researchers rely on to select an NGS provider.
- Publications – providers who are listed in publications involving similar projects.
- What kind of QC will be run on the sample.
- Overall experience indicators such as time in business and volume of samples regularly handled.
- Data and sample security.
- Location – this factor is considerably important if previous trust is not established. Some researchers have absolutely no problem shipping samples across the globe, while others might physically drive their samples to a local provider to ensure sample integrity.
We would love to hear your feedback on this topic whether you are an NGS provider, or a researcher actively using next sequencing. What other decision driving criteria have you found as a provider, or what are some other factors important to you as a researcher?
Life Technologies announced yesterday that they launched the Ion AmpliSeq Exome Certified Service Provider Program.
What the program is in a nutshell:
- Goals: Offer a network of next gen sequencing providers able to help researchers get a high quality exome sequence at a reduced cost with fast turnaround times and low amounts of input material
- Exome sequencing inputs: as little as 50ng of customer DNA
- Library kit used: Ion AmpliSeq Exome kit
- NGS Instrument used: Ion Proton
- Exome sequencing outputs: high quality data, which of course can be used with Ion Reporter Software for mutation validation, annotation, and reporting
The Service Provider Program is intended to fill exome sequencing market demand which Life Tech argues has been under-serviced with exome sequencing currently going for $1,000+ , long turnaround times up to 8 weeks, and requiring up to 3mg of DNA. Dr. Candace Johnson, Deputy Director and the Wallace Chair of Translational Research at Roswell Park Cancer Institute states “Exome sequencing will be central to discoveries made in clinical research”. If the Exome CSP delivers as promised, it could have a major impact in accelerating discoveries made in clinical research.
For more information on the Life Tech Provider Program please see the entire press release.
Oxford Gene Technology (NGS provider currently listed on Genohub) recently presented the results of their next gen sequencing survey which demonstrated targeted resequencing as the top use for next generation sequencing. The results are based on a survey of 596 researchers who responded regarding their current and expected use of NGS services. When compared to the results for whole genome sequencing the popularity of targeted resequencing is possibly attributed mostly to the lower cost of targeted resequencing. This infographic depicts the results:
OGT NGS Survey Results
Other interesting results point to a general data problem with 38% of respondents saying they lack trust in bioinformatics data. Bioinformatics also leads the field when researchers were asked about the biggest barrier to NGS usage (see below).
Barriers to NGS Usage
Undoubtedly this presents an immense opportunity for the bioinformatics sector to increase confidence in data accuracy and interpretation which could have a positive impact on the use of next gen sequencing as a whole.
You can find many more interesting survey results on the excellent infographic titled Oxford Gene Technology – NGS Survey 2013.
Genohub would like to welcome BaseClear to the Genohub family. The sequencing services listed by BaseClear has added more available options for researchers on the Genohub next generation sequencing market.
BaseClear has listed the following next gen sequencing instruments and Illumina library prep options:
- Illumina MiSeq paired end sequencing options
- Illumina HiSeq paired end sequencing options
- PacBio SMRT Cell
- Library prep:
- Illumina DNA
- Illumina 16S V4
- Illumina RNA (rRNA-depleted)
BaseClear is located in the BioSciencePark (BSP) of Leiden in the Netherlands. By using Illumina systems (HiSEQ2500 and MiSEQ) in combination with the PacBio RS system BaseClear can offer whole genome analysis and offer a wide variety of combinations of read lengths, number of tags and paired end size ranges. The lab has been ISO17025 accredited since 2006.
We are excited to include BaseClear’s high throughput sequencing services on the Genohub next gen sequencing market.
Genohub would like to welcome the Genome Sequencing Facility (GSF) at Greehey Children’s Cancer Research Institute in the University of Texas Health Science Center at San Antonio to the Genohub family. The sequencing services listed by UTHSCSA has added more available options for researchers on the Genohub next generation sequencing market.
UTHSCSA listed the following next generation sequencing instruments and Illumina library preparation options:
- Illumina MiSeq paired end sequencing options
- Illumina HiSeq single read and paired end sequencing options
- Library prep:
- Illumina ChIP
- Illumina Directional RNA (polyA-selected)
- Illumina Directional RNA (rRNA-depleted)
- Illumina DNA
- Illumina Exome
- Illumina RNA (polyA-selected)
- Illumina RNA (rRNA-depleted)
- Illumina Small RNA (microRNA)
The GSF has a stated mission to deploy NGS systems focusing on cancer genomics to benefit Greehey CCRI investigators and the wider research community. The NGS facility performs all protocols necessary for preparing a sample to be sequenced on the Illumina HiSeq 2000 system. The GSF is also a research group with experience in customizing experiments and developing new applications. They provide:
- Complete project consultation for optimal experimental design and setup
- Complete quality control analysis during library preparation and data generation
- Secure website to download the sequencing data with quality information
- Full project report
- Bioinformatics analysis option available
- NCBI GenBank submission option available
We are excited to include UTHSCSA high throughput sequencing services on the Genohub next generation sequencing market.