Don't Miss
  • Associate Professor
  • Using single-cell RNA sequencing to disentangle the blood system
  • Arriba – accurate and efficient detection of gene fusions from RNA sequencing data
  • MSRG – new database of mosquito small RNA transcriptomes
  • Single-cell RNA sequencing reveals SARS-CoV-2 infection dynamics in the lungs
  • Genuity Science wins 2021 BIG Innovation Award for novel approach to analysis of single-cell RNA sequencing data
  • CLInt-Seq – a method to more efficiently isolate and identify rare T cells
  • Re­sponse to in­fec­tion ther­apy bet­ter un­der­stood thanks to a new sequencing tech­nique
  • Cell atlas of tropical disease parasite may hold key to new treatments
  • The impact of gene annotation choice on the quantification of RNA-seq data

RNA-Seq BlogRNA-Seq Blog Transcriptome Research & Industry News

  • Home
  • News
    • Commentary
    • Headlines
    • Industry News
    • Grants / Funding
    • Information
    • Poll Results
    • Press Releases
    • Transcriptome Sequenced
  • Events
    • Conferences
    • Meetings
    • Webinars
    • Workshops
    • Projects
    • Local Events
  • Jobs
  • Technology
    • Methods
      • Workflow
      • RNA Extraction
      • Library Preparation
      • Sequencing Protocols
      • Statistical Analysis
      • Data Analysis
        • Analysis Pipelines
        • Annotation
        • Clouding Platforms
        • Data Normalization
        • Data Sets
        • Data Visualization
        • Databases
        • Expression and Quantification
        • Other Tools
        • Pathway Analysis
        • SNP Detection
        • Splicing and Junction Mapping
        • Statistical Analysis
        • Transcriptome Assembly Tools
        • Unspliced Mapping Tools
    • New Products
      • Our Advertisers
    • Patents
    • Presentations
    • Publications
    • Review Publications
    • Web Tools
  • Data Analysis
    • Analysis Pipelines
    • Annotation
    • Clouding Platforms
    • Data Normalization
    • Data Sets
    • Data Visualization
    • Databases
    • Expression and Quantification
    • Other Tools
    • Pathway Analysis
    • SNP Detection
    • Splicing and Junction Mapping
    • Statistical Analysis
    • Transcriptome Assembly Tools
  • Blog
  • Reader Posts
  • Contact
    • Administration
    • Contribute News
    • Subscribe
    • Advertise
    • Request for RNA-Seq Services

Tag Archives: ENDO 2018

New data suggests Veracyte’s RNA-Seq based Afirma GSC can help patients avoid unnecessary thyroid surgery

March 20, 2018 Leave a comment 2,014 Views

rna-seq

Veracyte, Inc. today announced that new data presented at ENDO 2018, the annual meeting of the Endocrine Society, suggest that the Afirma Genomic Sequencing Classifier (GSC) can help significantly more

Read More »

Stay Connected

RNA-SEQ & COVID-19

Publications Trend

Recent RNA-SEQ Pubs

Prepubertal exposure to a high dose of cadmium induces hypothalamic injury through transcriptome profiling alteration and neuronal degeneration in female rats.
Computationally reconstructing cotranscriptional RNA folding from experimental data reveals rearrangement of non-native folding intermediates.
Aethionema arabicum genome annotation using PacBio full-length transcripts provides a valuable resource for seed dormancy and Brassicaceae evolution research.
Genome-Wide Discovery of Natural Variation in Pre-mRNA Splicing and Prioritizing Causal Alternative Splicing to Salt Stress Response in Rice.
NOTCH3, a crucial target of miR-491-5p/miR-875-5p, promotes gastric carcinogenesis by upregulating PHLDB2 expression and activating Akt pathway.
HAND1 and BARX1 act as transcriptional and anatomic determinants of malignancy in gastrointestinal stromal tumor.

News in Pictures

rna-seq
rna-seq
rna-seq
rna-seq
rna-seq
rna-seq
rna-seq
rna-seq
rna-seq
rna-seq
rna-seq
rna-seq
rna-seq
rna-seq
rna-seq

recent visitors

Subscribe to the RNA-Seq Blog


Email Frequency

RNA-Seq Products & Services

Most Shared Posts

  • Comparative analysis of single-cell RNA sequencing platforms and methods
    Google +1 logo   Twitter logo   Facebook logo
  • Targeted transcriptome analysis uncovers previously unknown isoform reprograming in colon cancer
    Google +1 logo   Twitter logo   Facebook logo
  • PEARL-seq™ – systematically identify RNA-targeted small molecules
    Google +1 logo   Twitter logo   Facebook logo
  • New research identifies circulating RNA preeclampsia biomarkers
    Google +1 logo   Twitter logo   Facebook logo
  • NYIT researcher receives NHGRI grant to unlock mysteries in RNA sequencing
    Google +1 logo   Twitter logo   Facebook logo
  • Popular
  • Recent
  • Comments
  • rna-seq

    RPKM, FPKM and TPM, clearly explained

    July 22, 2015
  • rna-seq

    How to Analyze RNA-Seq Data?

    October 10, 2016
  • rna-seq

    Visualization of nucleotide substitutions in the (micro)transcriptome

    August 13, 2014
  • rna-seq

    Life Technologies Releases New Research Tool: Oncomine NGS RNA-Seq Gene Expression Browser

    April 8, 2014
  • rna-seq

    Comparison of TMM (edgeR), RLE (DESeq2), and MRN Normalization Methods

    October 6, 2016
  • rna-seq

    Associate Professor

    6 hours ago
  • rna-seq

    Using single-cell RNA sequencing to disentangle the blood system

    3 days ago
  • rna-seq

    Arriba – accurate and efficient detection of gene fusions from RNA sequencing data

    3 days ago
  • rna-seq

    MSRG – new database of mosquito small RNA transcriptomes

    4 days ago
  • rna-seq

    Single-cell RNA sequencing reveals SARS-CoV-2 infection dynamics in the lungs

    4 days ago
  • Ivan Molineris: If I understood well the annotation "ENSEMBL" used in this p...
  • Aashni: Nice article...
  • rna fixation: Wonderful article! We will be linking to this great article...
  • Protein Fixation: I was Searching Health blog commenting site the time I found...
  • SimPHARM.com: Great post, every thing is describe here very understandable...

Categories

Archives

What is RNA-Seq?

long RNAs are first converted into a library of cDNA fragments through either RNA fragmentation or DNA fragmentation. Sequencing adaptors (blue) are subsequently added to each cDNA fragment and a short sequence is obtained from each cDNA using high-throughput sequencing technology. The resulting sequence reads are aligned with the reference genome or transcriptome, and classified as three types: exonic reads, junction reads and poly(A) end-reads. These three types are used to generate a base-resolution expression profile for each gene. Nat Rev Genet 10(1):57-63 (2009)


RNA-Seq

Recent News

  • rna-seq

    Associate Professor

    6 hours ago
  • rna-seq

    Using single-cell RNA sequencing to disentangle the blood system

    3 days ago
  • rna-seq

    Arriba – accurate and efficient detection of gene fusions from RNA sequencing data

    3 days ago
  • rna-seq

    MSRG – new database of mosquito small RNA transcriptomes

    4 days ago
  • rna-seq

    Single-cell RNA sequencing reveals SARS-CoV-2 infection dynamics in the lungs

    4 days ago
  • rna-seq

    Genuity Science wins 2021 BIG Innovation Award for novel approach to analysis of single-cell RNA sequencing data

    4 days ago
  • rna-seq

    CLInt-Seq – a method to more efficiently isolate and identify rare T cells

    5 days ago

Subscribe to the RNA-Seq Blog


Email Frequency

Social Networking Pages


RNA-Seq
  • 6,481 Followers
  • 2,079 Fans
© Copyright 2009-2020, All Rights Reserved. | Designed by Go Big - Online Presence Creations