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There are 36 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, Genome, Gene, Genomic, NGS, Whole-Exome, Bioinformatics .

Start-ups (2)

Early-stage companies (20)

Established companies (13)

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

United States (13)

China (4)

Taiwan (4)

India (3)

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Novogene Novogene Corporation

early-stage

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

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

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

- Target 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 ...

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

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

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

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

- Target 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 ...

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

Aperiomics Aperiomics, Inc.

early-stage

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

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

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

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

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

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

Yourgene Bioscience

established

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

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

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

Plurk(Open New Window) Whole-Exome Sequencing Whole Exome Sequencing technology uses the sequence capture technology to sequence the whole exome region after capture ...

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

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

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

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

基因檢測 - 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 ...

- DNA 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 ...

能夠輔助何種臨床研究? 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 ...

Genome Consortium 等大型定序計畫,皆也透過Whole-Exome Sequencing等定序技術針對癌症做定序,透過生物資訊分析,發現與癌症相關的致病候選基因與點位,經過驗證與確效後可運用於臨床診斷與藥物開發。有鑑於此,Whole-Exome Sequencing也被喻為臨床診斷與治療決策之明日之星。

SOPHiA GENETICS SOPHiA GENETICS SA.

early-stage

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Contact Solutions WES SOPHiA Whole Exome Solution™ Focusing on what matters for rare and inherited diseases SOPHiA Whole Exome Solution is a genomic application

SOPHiA Exome Solutions include two genomic applications, Clinical and Whole Exome, that both bundle a smart capture-based target enrichment kit with the ...

applications targeting: • 4,490 genes for Clinical Exome • >19,000 genes for Whole Exome • Automated workflow available on leading liquid handling robots for ...

CNV detection available for: • 98.1% of Clinical Exome genes • 93.3% of Whole Exome genes UNIVERSAL PLATFORM • Intuitive and user-friendly interface • ...

generation Relevant gene content SOPHiA Clinical Exome Solution and Whole Exome Solution cover the coding regions (±5bp of exon-flanking regions) of 4 ...

input requirement 200 ng 12 Mb (Clinical Exome) Target region 39 Mb (Whole Exome) Library preparation time 2 days *Complete list of genes available ...

Recommended samples per run (for >50x coverage depth) Clinical Exome Whole Exome SP 48 (per lane) 12 S1 96 (per lane) 24 (per lane) S2 NA 56 (per

Paradigm4, inc.

established

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hereditary transthyretin-mediated (hATTR) amyloidosis in 302,330 UK Biobank whole exome sequences Mollie Plekan1, Margaret Parker1, Simina Ticau1, Lucas D. Ward1 ...

missense TTR variants in a cohort of 302,330 subjects with available whole exome sequence and to test their association with hATTR amyloidosis. Methods ...

Methods We identified missense TTR variants from 302,330 UK Biobank (UKBB) whole exome sequences Variants were classified as pathogenic, benign, conflicting ...

Conclusions Characterization of missense TTR variants in 302,330 UKBB whole exome sequences revealed support for the ‘benign’ designation of the Gly6Ser

predicted loss of function variants and 34 biomarkers in 255,873 UK Biobank whole exome sequences M. M. Parker, A. Deaton, J. Liu, L. D. Ward, A. O. Flynn-Carroll ...

29.2020 | Gene-level analysis of loss of function variants in 246,731 whole exome sequences reveals a novel association with diabetes A. Deaton, M. M. ...

with hereditary transthyretin mediated amyloidosis in 302,330 UK Biobank whole exome sequences M. Plekan, M. M. Parker, S. Ticau, L. D. Ward, A. Deaton, A

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