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There are 50 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 Sequencing, Genome, Exome, Bioinformatics, Gene, Genomics, NGS, Genetic .

Start-ups (5)

Early-stage companies (30)

Established companies (14)

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

United States (20)

China (4)

India (4)

Taiwan (4)

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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 Sequencing ...

Pre-made 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 ...

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

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

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

Pre-made 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 ...

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

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

BGI Group Shenzhen Huada Gene Technology Co., Ltd.

established

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GigaScience Press - Technology Disease Research Whole genome resequencing Whole Exome Sequencing Single Cell Sequencing Immune Repertoire Sequencing Plant and ...

Whole Genome Bisulfite Sequencing Library Prep Kit MGIEasy Exome Capture V4 Probe Set MGIEasy Exome Capture V5 Probe Set MGIEasy RAD Library Prep Kit MGIEasy ...

Set MGIEasy Exome FS Library Prep Set MGIEasy Exome Universal Library Prep Set MGIEasy FS PCR-Free DNA Library Prep Set MGIEasy RNA Exome Application MGIEasy ...

Sequencing Library Prep Set MGIEasy Exome Capture V5 Universal Reagent Kit MGIEasy stLFR Library Prep Kit Mgieasy exome capture V4 Universal Reagent Kit MGIEASY ...

Shenzhen(518083) Technology Disease Research Whole genome resequencing Whole Exome Sequencing Single Cell Sequencing Immune Repertoire Sequencing Plant and ...

Indel, CNV and SV. - Whole Exome Sequencing The exome is the protein-coding region of the human genome. Although the exome region is less than 2% of the

GigaScience Press - Technology Disease Research Whole genome resequencing Whole Exome Sequencing Single Cell Sequencing Immune Repertoire Sequencing Plant and ...

Whole Genome Bisulfite Sequencing Library Prep Kit MGIEasy Exome Capture V4 Probe Set MGIEasy Exome Capture V5 Probe Set MGIEasy RAD Library Prep Kit MGIEasy ...

Set MGIEasy Exome FS Library Prep Set MGIEasy Exome Universal Library Prep Set MGIEasy FS PCR-Free DNA Library Prep Set MGIEasy RNA Exome Application MGIEasy ...

Sequencing Library Prep Set MGIEasy Exome Capture V5 Universal Reagent Kit MGIEasy stLFR Library Prep Kit Mgieasy exome capture V4 Universal Reagent Kit MGIEASY ...

gene hereditary diseases, 1,445 types of gene detection and clinical full-exome detection. . Based on scientific and rigorous genomics research and accurate

1010Genome

early-stage

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sales@1010genome.com - Home - Sequencing Services - Genome Sequencing - Exome Seq - Exome SNP Calling Accuracy - RNA Seq - Genome Assembly - Biodiversity ...

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

study genetic disease variants, cancer biomarker and population studies. Exome accounts for just a 2% of total genome size that makes it easier to generate ...

a 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 ...

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

sales@1010genome.com - Home - Sequencing Services - Genome Sequencing - Exome Seq - Exome SNP Calling Accuracy - RNA Seq - Genome Assembly - Biodiversity ...

Category: Whole Exome Sequencing Home Category: Whole Exome Sequencing 1010Genome Presents Next Generation Sequencing and Whole Exome Sequencing Services ...

whole exome sequencingAdmin 1010Genome is a providers of high quality whole exome sequencing services for research labs and routine clinical exome screening ...

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

Pipeline - RNA Sequencing - Sequence Assembly - Transcriptome Analysis - Whole Exome Sequencing - Whole Genome Sequencing Archives - December 2019 - November

Toldot Genetics Toldot Genetics Limited

early-stage

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Toggle navigation Exome-Seq + Full Analysis for $1000 Get full bioinformatics report including short-list of candidate variants (Special discount for ...

of sequencing studies in human genetics (Nat Rev Genetics 2013) - Whole Exome Sequencing for healthy adults (PNAS 2013) Send Theme by Pojo.me - WordPress

Paradigm4, inc.

established

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stockholder Cases of acute hepatic porphyria in the UK Biobank: insights from exome sequencing Alexander O. Flynn-Carroll, Lucas D. Ward, Margaret M. Parker ...

and array genotyping data; subsets also have primary care data and whole-exome sequences. Inpatient hospitalization diagnosis of “other porphyria” (ICD10 ...

NOS.” Exome sequencing data was available for 454,787 individuals in the UKBB, and we used these data to investigate AHP-causing genes in 29 exome-sequenced ...

damaging missense variants. Patient History and Exome Analysis Individual Diagnosis Suspected Causal Exome Variants 1 C3715 Coproporphyria 2 Cyu8H Other ...

[P, D] Yellow = Complex clinical cases that are likely AHP in light of exome data but have evidence of misdiagnosis Blue = Other high-confidence AHP cases: ...

inpatient E80.2 code plus exome variant C We found potentially causal AHP variants in 13 of the 29 individuals with exome data. Four individuals had

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 ...

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

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

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