TACGenomics
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Encino, California, US
TACGenomics is a genomic service company based in California USA, providing comprehensive solution to the problem of handling data generated by next generation sequencing (NGS) devices. TACGenomics has a team composed of bioinformatician, molecular biologist and computer scientist who are all at Ph.D. level.... Show more »
TACGenomics is a genomic service company based in California USA, providing comprehensive solution to the problem of handling data generated by next generation sequencing (NGS) devices. TACGenomics has a team composed of bioinformatician, molecular biologist and computer scientist who are all at Ph.D. level. Our team has the experience of hundreds of NGS data analysis projects from all over the world. The mission of TACGenomics is to help our customer to solve the biological questions. After computation analysis completed by the bioinformatician, our molecular biologist will interpret the analyzed data carefully, provide more insight into your project and help the publication of the project in the high impact journal.
RNA-seq (RNA sequencing), also called whole transcriptome sequencing, uses next-generation sequencing (NGS) to reveal the presence and quantity of RNA in a biological sample at a given moment in time.
TACGenomics use the cutting-edge pipeline to analyze your RNA-seq data. We put more attention to quality control and data... Show more »
RNA-seq (RNA sequencing), also called whole transcriptome sequencing, uses next-generation sequencing (NGS) to reveal the presence and quantity of RNA in a biological sample at a given moment in time.
TACGenomics use the cutting-edge pipeline to analyze your RNA-seq data. We put more attention to quality control and data visualization.
The services for RNA seq data analysis includes:
Exome sequencing is a cost-effective approach when whole-genome sequencing is not practical or necessary. It is a quick and effective strategy to identify disease-causing genes for rare Mendelian disorders. It is also being applied to profile all variants in complex diseases such as Cancer and Diabetes.
TACGenomics use the... Show more »
Exome sequencing is a cost-effective approach when whole-genome sequencing is not practical or necessary. It is a quick and effective strategy to identify disease-causing genes for rare Mendelian disorders. It is also being applied to profile all variants in complex diseases such as Cancer and Diabetes.
TACGenomics use the cutting-edge pipeline to analyze your Exome-seq data. We put more attention to quality control and data visualization. (see our work)
The services for RNA seq data analysis includes:
Germline SNV/Indel calling for individual sample
Somatic SNV/Indel/copynumber calling for paired samples
De novo germline variants calling in trio studies
Variant phenotype association test
CoMut and Circos plotting (if appliable)
SNV/Indel calling for Whole genome sequencing
ChIP-seq is a method which combines chromatin immunoprecipitation(ChIP) with massively parallel DNA sequencing to identify the binding sites of DNA-associated proteins.ChIP-seq is used primarily to determine how transcription factors and other chromatin-associated proteins influence phenotype-affecting mechanisms.
TACGenomics... Show more »
ChIP-seq is a method which combines chromatin immunoprecipitation(ChIP) with massively parallel DNA sequencing to identify the binding sites of DNA-associated proteins.ChIP-seq is used primarily to determine how transcription factors and other chromatin-associated proteins influence phenotype-affecting mechanisms.
TACGenomics use the cutting-edge pipeline to analyze your Chip-seq data. We put more attention to quality control and data visualization.
The services for RNA seq data analysis includes:
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