Advertise

Get your product or service in front of targeted visitors.

Our visitors are YOUR potential customers. Ensure that your business name is seen – and remembered – by as many researchers as possible.

Why Blog Advertising?

The RNA-Seq Blog has dynamic keywords, extensive SEO optimization and is updated daily by the administrator and or blog readers. This means, the RNA-Seq Blog receives more targeted search engine visitors more frequently than static html sites.

Blog readers tend to be extremely interested in the topic and very attached to the blogger. You can’t ask for a better community of users to be in front of.

Your ads successfully reach niche audiences for a fraction of the cost of traditional advertising.

Site Metrics

>50,000 Feed Subscribers

~35,000 Unique Visitors / Month

~90,000 Hits / Month

We have a Google pagerank of 5 and our metrics are trending up quickly.

Do a quick Google search of the keyword “RNA-Seq” and see our high ranking in the organic search results.

rna-seq

Advertising Opportunities

We offer a range of advertising opportunities to fit YOUR campaign…

Email us at: admin@rna-seqblog.com

Join the growing list of RNA-Seq Blog advertisers.

1CellBio 1CellBio Announces Custom Targeted Bead Program to Accelerate Next Phase in Single-Cell Analysis

1CellBio today announced a new program to supply select customers with its proprietary inDrop™ hydrogel beads synthesized with custom primers that target user-specified transcripts. “This new program enables researchers to focus their sequencing depth on their genes of interest rather than the full transcriptome,” said Colin J.H. Brenan, PhD, Chief Executive Officer at 1CellBio. “We ...

Lexogen Lexogen announces the launch of the CORALL Total RNA-Seq Library Prep Kit

Today Lexogen announced the launch of the CORALL Total RNA-Seq Library Prep Kit. This new all-in-one library prep kit can be used for all whole transcriptome analysis applications such as differential expression, isoform quantification, single nucleotide polymorphism (SNP), and mutation detection. “RNA-Seq library preparation protocols are still plagued by biased read distribution. Especially start sites are ...

Dolomite Dolomite Bio unveils new scRNA-Seq Reagent Kit at AGBT 2019

Dolomite Bio, a leading provider of cutting-edge single cell technologies, today announced the launch of a new scRNA-Seq Reagent Kit to expand the Nadia Instrument portfolio. This convenient and cost-effective option is being showcased at the Advances in Genome Biology and Technology 2019 General Meeting (AGBT2019) – February 27th to March 2nd in Marco Island, ...

Norgen Norgen Biotek Achieves Illumina Propel Certification as a Service Provider for Next Generation Sequencing

Norgen Biotek Corp., an innovative privately held Canadian biotechnology company focusing primarily on nucleic acid and protein stabilization and purification, as well as providing high quality services to the scientific community, today announced that it has become Propel-Certified through Illumina as a Next Generation Sequencing (NGS) service provider.  Norgen’s Propel Certification covers both the NextSeq ...

Amaryllis Amaryllis Nucleics Adds Dual-Indexing Capabilities to its Dual-Mode RNAseq Kit

Amaryllis Nucleics, a Bay Area biotech company using the most advanced chemistry for RNA sequencing sample prep to provide rapid and accurate RNA sequencing, today launched a new version of their dual-mode (FT+3′-DGE) RNA-seq kit that allows users to do dual-indexed sequencing. The YourSeq Dual RNAseq Library Kit is a versatile, Illumina-compatible RNAseq library kit that can ...

QIAGEN QIAGEN Launches Novel RNA-Seq Library Preparation Solutions for Next-Generation Sequencing

QIAGEN today announced the launch of a breakthrough technology enabling faster, simpler library preparation for RNA sequencing. A key element of this portfolio is the QIAseq FastSelect RNA Removal Kit which provides a novel solution for scientists to target RNA types that are irrelevant to their research and remove them from RNA-seq libraries for next-generation ...

Lexogen Lexogen and Bluebee Collaborate to Streamline QuantSeq-UMI Sequencing Data Analysis Pipeline

Lexogen, a transcriptomics and next-generation sequencing company and Bluebee, a global bioinformatics platform, have announced today the implementation of QuantSeq Unique Molecular Identifiers (UMI) data analysis pipeline on the Bluebee genomics analysis platform. This collaboration offers QuantSeq users utilizing UMIs the opportunity to analyze samples in a convenient and rapid manner without the need for ...

SomaGenics SomaGenics announced the launch of RealSeq®-biofluids

SomaGenics launches its RealSeq®-biofluids kit and advances liquid biopsy development with new NIH funding for cf-miRNA NGS technology Santa Cruz, CA, May 2018 – SomaGenics announced the launch of RealSeq®-biofluids, a next-generation sequencing (NGS) library construction kit sensitive enough to detect small RNAs from cell-free biofluids. Further enhancing its efforts in the liquid biopsy arena, ...

NuGEN NuGEN Introduces Unique Indexing Solutions for Illumina’s High Capacity Sequencing Platforms

Today NuGEN Technologies announces a new line of indexing solutions designed to enable researchers to take full advantage of the latest generation of Illumina sequencers. The three new enhancements include the launch of 96 unique dual index pairs to address index hopping, the incorporation of molecular tags to accurately measure PCR duplication levels, and the ...

Qlucore Qlucore launches Omics Explorer 3.3

Qlucore, a leader in the development of bioinformatics visualization software, has today launched the latest version of its advanced data analysis software. Qlucore Omics Explorer 3.3 includes a new Next Generation Sequencing (NGS) Module and additional new functionalities. Qlucore Omics Explorer is a next-generation bioinformatics software program for broad usage, known for its easy to ...

Lexogen Lexogen Expands the Product Portfolio of RNA-Seq Kits with the Launch of a New Small RNA-Seq Library Prep Kit

Ever since small RNA (sRNA) was found to play key functional roles in the regulation of gene expression, researchers have taken special interest in the group of non-coding sRNAs such as microRNA (miRNA) and small interfering RNA (siRNA). miRNA from liquid biopsy samples (i.e. plasma, serum, and urine) have been of particular interest for their ...

Norgen Norgen Biotek has launched a new Small RNA Library Prep Kit and new portfolio of RNA Sequencing Services

Norgen Biotek Corp., an innovative Canadian biotechnology company focusing primarily on advancing powerful tools for nucleic acid and protein purification and stabilization, today announced the recent launch of their new portfolio of product and service solutions for Next Generation Sequencing (NGS) applications. Norgen has extensive experience with NGS, and has leveraged this expertise to develop ...

Lexogen Lexogen Launches Quantitative RNA-Seq Service for Cost-efficient and Accurate Gene Expression Profiling

Lexogen, a transcriptomics and next generation sequencing company, has announced the start of its RNA-Seq service, which focuses on gene expression profiling using Lexogen’s proprietary QuantSeq technology. Lexogen’s QuantSeq 3′ mRNA-Seq Library Prep Kit has already been recognized as one of the fastest, most cost-efficient, and accurate methods for expression profiling using next generation sequencing. Analysis ...

A A new workflow for single cell sequencing reduces the cost of sample prep by 90%

TTP Labtech Ltd, a global leader in the design and development of automated instrumentation and consumables for life science applications, and the University of California San Diego (UC San Diego), have announced that their collaboration has resulted in a new workflow for single cell sequencing, which reduces the cost of sample preparation by 90%. The ...

Illumina Illumina

Illumina Next-Generation Sequencing Platforms Illumina offers innovative next-generation sequencing (NGS) platforms that deliver industry-leading data quality and accuracy, at an unparalleled scale. With flexible throughput and simple, streamlined workflows, our sequencing platforms are transforming the field of genomics. Illumina technology empowers more and more NGS users every day. NGS has transformed the genomics community to ...

Life Life Technologies

Life Technologies offers two great options for transcriptome analysis: Whole transcriptome sequencing, or RNA-Seq, for both discovery and gene expression analysis. Use the Ion Proton™ System combined with Ambion® RNA purification and Ion Torrent™ library construction kits for identification and quantitation of both known and novel transcripts, including gene fusions and splice variants. Ion AmpliSeq™ ...

Fluidigm

Fluidigm – The C1™ Single-Cell Auto Prep System is a new approach to single-cell genomic applications, including targeted gene expression and the new mRNA sequencing protocol for transcriptome analysis of single cells. http://www.fluidigm.com/c1system.html

Agilent Technologies

Agilent Technologies – Agilent’s SureSelect market leading platform provides a complete portfolio of catalog and custom products, providing the flexibility you need, for your discovery to follow-up studies. New HaloPlex products combine the speed of PCR with the sensitivity of hybridization providing a robust solution for targeting smaller capture regions. http://www.genomics.agilent.com/CollectionOverview.aspx?PageType=Application&SubPageType=ApplicationOverview&PageID=2094&CID=G0961  

Epicentre (an Illumina company)

 – The Ribo-Zero™ Magnetic Gold Kit (Epidemiology) combines Epicentre’s Ribo-Zero™ Gold (Human/Mouse/Rat) and Ribo-Zero™ (Bacteria) rRNA removal reagents into a single solution that effectively removes rRNA, including human mitochondrial RNA, from samples composed of both human/mouse/rat and bacterial RNA. http://www.epibio.com/products/rna-sequencing/rrna-removal/ribo-zero-magnetic-gold-kit-%28epidemiology%29

NuGEN Technologies

NuGEN Technologies – The Ovation Ultralow Methyl-Seq Library Systems provide a simple, fast and scalable solution for producing libraries used in conjunction with bisulfite sequencing to analyze DNA methylation. The system requires as little as 10 ng of DNA, thereby enabling methylation studies with a broad range of sample types. The protocol is compatible with ...