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There are 40 companies in the field of Bioinformatics on spotfolio that produce or deliver products, that utilize or research technologies or that are otherwise engaged in topics such as Exome, Sequencing, Gene, Genome, Genomic, Bioinformatics, Genetic, Exome-Sequencing .

Start-ups (3)

Early-stage companies (23)

Established companies (14)

The majority of these companies is located in the following countries.

United States (15)

China (4)

India (4)

Taiwan (4)

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Novogene Novogene Corporation

early-stage

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Capture Sequencing Back - Human Whole Exome Sequencing - Mouse Whole Exome Sequencing - Clinical Whole Exome Sequencing (CLIA/CAP) - Target Region Sequencing ...

Library Sequencing Back - Clinical Diagnostics Back - Clinical Whole Exome Sequencing (CLIA/CAP) - Clinical Panels Back - Genetic Testing Back - Oncology ...

Discovery and Pre Clinical Back - Whole Genome Sequencing Back - Whole Exome Sequencing Back - RNA-Seq Back - FFPE RNA-seq Back - Small RNA Sequencing Back ...

Capture Sequencing - Human Whole Exome Sequencing - Mouse Whole Exome Sequencing - Clinical Whole Exome Sequencing (CLIA/CAP) - Target Region Sequencing ...

- Pre-made Library Sequencing Clinical Diagnostics Clinical Whole Exome Sequencing (CLIA/CAP) Clinical Panels - Genetic Testing - Oncology - NovoPM™ ...

Services Discovery and Pre Clinical - Whole Genome Sequencing - Whole Exome Sequencing - RNA-Seq - FFPE RNA-seq - Small RNA Sequencing - Pacbio Sequencing

Capture Sequencing Back - Human Whole Exome Sequencing - Mouse Whole Exome Sequencing - Clinical Whole Exome Sequencing (CLIA/CAP) - Target Region Sequencing ...

Library Sequencing Back - Clinical Diagnostics Back - Clinical Whole Exome Sequencing (CLIA/CAP) - Clinical Panels Back - Genetic Testing Back - Oncology ...

Discovery and Pre Clinical Back - Whole Genome Sequencing Back - Whole Exome Sequencing Back - RNA-Seq Back - FFPE RNA-seq Back - Small RNA Sequencing Back ...

Capture Sequencing - Human Whole Exome Sequencing - Mouse Whole Exome Sequencing - Clinical Whole Exome Sequencing (CLIA/CAP) - Target Region Sequencing ...

- Pre-made Library Sequencing Clinical Diagnostics Clinical Whole Exome Sequencing (CLIA/CAP) Clinical Panels - Genetic Testing - Oncology - NovoPM™ ...

Services Discovery and Pre Clinical - Whole Genome Sequencing - Whole Exome Sequencing - RNA-Seq - FFPE RNA-seq - Small RNA Sequencing - Pacbio Sequencing

1010Genome

early-stage

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Whole Exome Sequencing Exome Sequencing Data Analysis Variants in exome account for 85% of known disease variants. This makes exome sequencing one of ...

comprehensive sequencing coverage for variant identification. Focused exome sequencing approach can enable research teams to make optimal use of resources ...

towards a causal phenotype. Exome Sequencing provides a cost and time effective alternate to whole genome sequencing. Exome Sequencing is fast, cost effective ...

analysis. Human exome sequencing generated about 5 Gb of data as compared to 90Gb per whole genome. Over streamlines exome sequencing data analysis pipelines ...

a sample within hours and multiple samples per day. Why chose our Exome Sequencing Services? - Top quality sequencing data generated on Illumina HiSeq ...

experts handles your exome sequencing data. - Cost effective and quick turnover time. Exome Seq Data Analysis - Robust Exome sequencing data analysis pipelines

Eukaryotic genome annotation - About Us Category: Exome Sequencing Home Category: Exome Sequencing A Timeline of Steep Fall in Human Genome Sequencing ...

sequencing platform. The cost effective, optimized solutions for whole exome sequencing are critical for complex disease studies to discover SNP biomarkers ...

Service Provider? October 10, 2018No Commentsbioinformatic analysis, exome sequencing cost, rna seq data, whole genome sequencingAdmin While the costs towards ...

of whole… Read More Why Get Exome Sequencing Done? April 25, 2018No Commentsbioinformatic analysis, exome sequencing, Illumina sequencingAdmin For ...

For those who have non-medical background, exome sequencing is a method of studying an individual’s exome which account for about 85% of medical conditions ...

sequencing - Bioinformatic analysis - blog1 - de novo genome assembly - Exome Sequencing - Genome Sequencing - Illumina Sequencing - Metagenomic Analysis -

Yourgene Bioscience

established

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Yourgene Health分佈 - Human Genome Sequencing - DNA Resequencing - Whole-Exome Sequencing - DNA De Novo Sequencing - Targeted Sequencing(臨床研究) - Targeted Sequencing ...

Yourgene Health分佈 - Human Genome Sequencing - DNA Resequencing - Whole-Exome Sequencing - DNA De Novo Sequencing - Targeted Sequencing(臨床研究) - Targeted Sequencing ...

Whole-Exome Sequencing 字級: 小字級 中字級 大字級 分享: 分享到我的Facebook(開新視窗) 分享到我的Twitter(開新視窗) 分享到我的Google Plus(開新視窗) 分享到我的Plurk(開新視窗) Whole-Exome Sequencing - Human ...

Resequencing - Whole-Exome Sequencing - DNA De Novo Sequencing - Targeted Sequencing(臨床研究) - Targeted Sequencing Whole-Exome Sequencing 能夠輔助何種臨床研究? Whole-Exome ...

Whole-Exome Sequencing 技術,於臨床運用上不僅能夠作為快速定位單基因致病疾病的有力工具,也能應用研究多基因/點位變異的複雜疾病,如糖尿病、高血壓和腫瘤等。 如今,有許多大型的定序計畫, 採用Whole-Exome Sequencing技術,找尋SNPs/SNVs、結構變異 (SV)等,例如:美國國家衛生研究院 ...

Health,NIH)心肺血液研究所 (National Heart, Lung, and Blood Institute, NHLBI),便是利用(Exome Sequencing Project,ESP)定序計畫 ,探索各種與心臟、肺臟與心血管相關疾病之基因與功能作用機制。 除此之外,美國 The Cancer

Publications - Clinical & Research - Clinical Services Overview - Whole-Exome Sequencing - Targeted Sequencing - circulating cell free DNA - Genetic Testing ...

Publications - Clinical & Research - Clinical Services Overview - Whole-Exome Sequencing - Targeted Sequencing - circulating cell free DNA - Genetic Testing ...

prenatal screen - Sage Link - Home - Clinical & Research - Whole-Exome Sequencing Previous Page Font size: Small Medium Large Share to: Share to Facebook(Open ...

Plus(Open New Window) Share to Plurk(Open New Window) Whole-Exome Sequencing Whole Exome Sequencing technology uses the sequence capture technology to sequence ...

scientists. Under the same cost framework for sequencing, the whole exome sequencing technology can obtain greater coverage and more accurate data in the ...

therefore preferred by many researchers as an alternative. Thus, the Whole Exome Sequencing technology has become a useful clinical tool for sequencing the cell

Clevergene

early-stage

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methodologies for detecting Copy Number Variations (CNVs) from Human Exome sequencing data. - Tumblr - Pinterest - Google+ - E-Mail About The Author Leave

methodologies for detecting Copy Number Variations (CNVs) from Human Exome sequencing data. - October 23, 2015 - cleveradmin - No Comments - News Functional

Aperiomics Aperiomics, Inc.

early-stage

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medical management and genetic counseling options pre- and post-whole exome sequencing for patients with positive and negative results Margret Matias 1 ...

medical management and genetic counseling options pre- and post-whole exome sequencing for patients with positive and negative results Margret Matias et ...

Clipboard Full-text links Cite Display options Format Abstract Whole exome sequencing (WES) is expected to impact patient management, but data surrounding ...

management; whole exome sequencing. © 2019 National Society of Genetic Counselors. Similar articles - Clinical whole-exome sequencing results impact medical ...

additional but limited clinical utility compared with reanalysis of whole-exome sequencing. Alfares A, Aloraini T, Subaie LA, Alissa A, Qudsi AA, Alahmad A, Mutairi ...

29565419 - Not the End of the Odyssey: Parental Perceptions of Whole Exome Sequencing (WES) in Pediatric Undiagnosed Disorders. Rosell AM, Pena LD, Schoch

care following rapid mitochondrial genome sequencing in tandem with exome sequencing. Akesson LS, Eggers S, Love CJ, Chong B, Krzesinski EI, Brown NJ, Tan ...

1038/s41431-019-0477-3. Epub 2019 Jul 29. Eur J Hum Genet. 2019. PMID: 31358953 - Exome sequencing and whole genome sequencing for the detection of copy number variation

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