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There are 31 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, NGS, Gene, Genomics, Exome, Next-Generation-Sequencing, Generation-Sequencing, Indels .

Start-ups (1)

Early-stage companies (16)

Established companies (14)

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

United States (12)

Taiwan (4)

China (2)

India (2)

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ATGENOMIX Atgenomix Inc.

early-stage

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DeepVariant germline SNPs and indels variant calling by deep neural network GATK4 HaplotypeCaller germline SNPs and indels calling via local re-assembly ...

split-read analysis Tumor-Normal Somatic Analysis Mutect2 somatic SNVs and indels calling via local assembly of haplotypes Varscan2 somatic mutation calling

FASMAC

established

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aligned bases.", "# indels per 100 kbp" : "is the average number of indels per 100000 aligned bases.", "# indels" : "is the number of indels in all aligned ...

aligned bases", "# short indels" : "is the number of indels of length less or equal to 5 bp", "# long indels" : "is the number of indels of length greater than ...

than 5 bp", "Indels length" : "is the number of total bases contained in all indels", "# genes" : "is the number of genes in the assembly (complete and partial)

HEALTH IN CODE

established

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validity of Health in Code’s NGS panels has been demonstrated for SNPs and INDELs (≤20 pb) utilizing a NA 12878 (Coriell Cell Repositories, NJ) standard reference ...

000 sensitivity, 1.000 specificity, and 0.999 accuracy for both SNPs and INDELs, as well as high repeteability and reproducibility scores (≈96%) for variant

1010Genome

early-stage

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pipelines for reliable and sensitive detection of coding variants – SNPs and INDELS. - Team of experts handles your exome sequencing data. - Cost effective ...

Analysis - Robust Exome sequencing data analysis pipelines to identify SNPs, INDELS, CNV and other structural variants from your exome sequencing datasets. ...

pipeline. We have optimised various tools and parameters to detect SNPs, INDELS and CNVs in your exome sequencing data. Whole Exome Sequencing Service

Identification – Quality analysis with low false positive / negative SNPs and INDELS - Differential Gene Expression – Tailored analysis based on experiment design ...

Sequencing Robust Exome sequencing data analysis pipelines to identify SNPs, INDELS, CNV and other structural variants /rna-seq/ RNA Sequencing / Gene Expression ...

Variation Analysis Use our robust pipelines to identify structural variants – INDELS, CNVs and STRs using short reads or long reads data for your genomic studies

Mission Bio Mission Bio, Inc.

early-stage

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platform to simultaneously detect single nucleotide variants (SNVs) and indels from the same cell. Move beyond the average readout from conventional bulk ...

STUDY Applications Workflow DATASETS RESOURCES Why Single Cell for SNVs and Indels? The average readout from conventional bulk sequencing misses the underlying ...

populations. Single-cell DNA sequencing for single nucleotide variants and indels provides the true measure of clonal heterogeneity without inferring or guessing

relapse The only comprehensive single-cell DNA platform Identify SNVs, indels, CNVs, LOH, and translocations from the DNA of thousands of individual cells ...

Hotspot Learn how a custom single-cell panel can be used to co-detect SNVs, indels, CNVs, and proteins from the same cell in AML samples in a single workflow

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