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学术海报

Takara定期参加各种学术会议,展示我们卓越的NGS解决方案。以下是NGS海报资源,展示了Takara的NGS 应用的方法和数据。

 
全转录组分析(Whole transcriptome analysis)
单细胞 mRNA-seq

·Pushing the limits of single-cell RNA-seq with SMART-Seq single cell technology (ABRF, March 2020)

·Robust and sensitive detection of gene fusions using high-throughput SMART-Seq chemistry on the ICELL8 cx system (AGBT, Feb 2020; ABRF, March 2020)

·SMART-Seq Stranded Kit performance with ovarian cancer cells (ABRF, March 2019)

·A SMARTer solution to stranded single-cell RNA-seq (ABRF, April 2018)

·SMART-Seq v4 Ultra Low Input RNA Kit for the Fluidigm C1 System: improved chemistry for single cell transcriptome studies (NIH Single Cell Analysis Program Investigators Meeting, March 2016)

·Achieving unparalleled sensitivity and reproducibility in single-cell transcriptomics (ABRF, February 2016)

·An improved cDNA library generation protocol for transcriptome analysis from a single cell (ABRF, March 2014)

·Evaluation of commercially available RNA amplification kits at subnanogram input amounts of total RNA for RNA-seq (ABRF, March 2013)

 
Total RNA-seq

·SMART ligation-free tools for sequencing coding and non-coding RNA from low input samples (Keystone Symposia, February 2017)

·A complete solution for generating stranded RNA-seq libraries from high-input total RNA (ABRF, March 2015)

·SMART tools for strand-specific transcriptome analysis from mammalian total RNA (Keystone Symposia, March 2015)

·Strand-specific transcriptome sequencing for challenging samples (ABRF, March 2014)

·Development of a modified SMART system for robust transcriptome library preparation from limited quantities of compromised samples (ABRF, March 2013)

 
高通量自动化单细胞分析系统
·Automation and miniaturization of low-input RNA-seq sample prep on the Mantis platform (SLAS, January 2016)
 
目标区域测序分析(Targeted sequencing)
免疫组库分析(Immune profiling)

·Efficient high-throughput sequencing for quantitative immune profiling using unique molecular identifiers (ABRF, March 2020)

·High throughput single cell T-cell receptor profiling by SMART technology (AGBT, February 2018)

·A SMARTer approach to profiling the human T-cell receptor repertoire using the ICELL8 single-cell system (Royal Society of Chemistry, Single-Cell Genomics Meeting; September 2016)

·Single-cell T-cell receptor profiling with SMART technology (HudsonAlpha Immunogenomics Conference, September 2016)

·Profiling human TCR repertoire diversity with SMART technology (CAR-TCR Summit, September 2016)

·A SMARTer approach to profiling the human T-cell receptor repertoire (AAI, May 2016)

·A SMARTer approach to profiling the human T-cell receptor repertoire (ABRF, February 2016)

 
Small RNA-seq

·Ligation-free small RNA sequencing libraries from clinical samples using SMART technology (Liquid Biopsies and Minimally-Invasive Diagnostics; September 2016)

 
Targeted RNA-seq

·A SMARTer approach to gene fusion identification (Next Generation Dx Summit 2017, August 2017)

·Sensitive capture of full-length transcript information with targeted RNA-seq (ASHG, October 2016)

 
DNA-Seq分析
cfDNA来源的DNA-Seq

·ThruPLEX HV: a simplified system for preparation of molecular-tagged NGS libraries from FFPE and cell-free DNA (AMP, November 2019; AGBT, February 2020; ABRF, March 2020)

·Confident detection of low-frequency mutations in cell-free DNA using ThruPLEX technology with unique molecular tags (ABRF, April 2018)

·NGS libraries from cell-free DNA containing molecular tags prepared with ThruPLEX technology improve ability to detect rare alleles (ABRF, March 2017)

 
ChIP-seq

·Harnessing template-switching technology for preparation of low-input ligation-free sequencing libraries (ABRF, March 2015)

·Harnessing template-switching technology for ChIP-seq applications (CSHL Epigenetics & Chromatin, September 2014)

 
单细胞DNA-seq

·Next-generation whole genome amplification methods for CNV and SNV detection from single cells (Molecular Med Tri-Con, March 2019)

·PicoPLEX Gold: a new generation of single cell NGS library with high reproducibility, and greatly improved coverage and fidelity for precision medicine (AMP, October 2018)

·Sequencing single human cells and bacterial DNA using PicoPLEX DNA-seq at low coverage for aneuploidy, CNV, and genotyping applications (AGBT, February 2014)

 
全外显子测序(Whole exome sequencing)
·ThruPLEX as a high sensitivity library prep tool for whole exome and target panel sequencing (ASHG, September 2014)
 
高通量自动化DNA-seq
·Utilizing the Rheonix NGS OnePrep Solution to automate the Takara Bio ThruPLEX Tag-Seq HV library preparation kit (ABRF, March 2020)
 
 

页面更新:2022-03-15 09:41:57