AccuraScience, LLC is a bioinformatics company that provides NGS data processing, analysis and interpretation services. We serve academic research laboratories, medical facilities and third-party biotech companies. We perform all types of analysis routine and customized- that involve any types of NGS data produced from any sequencing platforms, and for any established and novel applications. We have a flexible payment schedule which includes three different tracks to meet your needs.
The company has been established and managed by a group of professional bioinformaticians, bioinformatics software developers and investors, with a mix of strong expertise in academic research, industrial development and business operation. Our NGS analysis service team is headed by seven Lead Bioinformaticians, with more than 70 years experience in bioinformatics research and development, and 25 years experience in NGS data analysis. They are supported by a team of bioinformatics engineers, IT specialists and customer support staff. Our team is dedicated to perfecting NGS analysis pipelines for all types of common and specialized applications.
We provide bioinformatics services to biomedical researchers in academic institutions, biotech and pharmaceutical industries, clinical facilities and government agencies. In addition to providing advice and assistance in the design and the implementation of bioinformatics-heavy research projects, our bioinformatics team directly carries out bioinformatics projects and bioinformatics-heavy components of research projects for our clients. We serve researchers and in diverse domains involving a wide range of organisms - from medical research using human samples or involving human patients, to animal and plant studies using model or non-model organisms, all the way to research projects focusing on microbial and viral species.
We undertake a wide variety of types of bioinformatics work, including but not limited to: processing, analyzing and interpreting high-throughput biological and medical data - with emphasis on next-generation sequencing (NGS) data, genomics, transcriptomics, proteomics, metabolomics and other omics data, statistical data analysis, data integration for diverse biomedical and other data types - e.g., for purposes of identifying causal relationships or other hidden information between measured variables, statistical modeling, machine learning method development and applications, metagenomics, ecology, phylogenetics, population genetics and other analyses related to evolutionary biology, data mining, customized and advanced analysis method development, specific data structure and algorithm development, informatics, database development and maintenance, software solutions, and IT and infrastructure solutions.
Our team is experienced in handling NGS data from all common platforms - including Illumina, Ion Torrent, 454, SOLiD and PacBio, and for all common NGS applications - including whole-genome sequencing (mapping-based or assembly-based applications), exome and other targeted sequencing, RNA-seq (mapping-based or de novo assembly-based analysis), ChIP-seq (for transcription factors, RNA PolII and histone modifications), and various sequencing-based DNA methylation applications. We are also experienced in less frequently used NGS applications such as DNase-seq, CLIP-seq, 4C-seq, Hi-C, ChIA-PET, and immunosequencing. Furthermore, we are also capable of assisting in developing novel NGS applications.
We are experienced in handling microarray data from all major array platforms (Affymetrix, Agilent, Illumina and NimbleGen), for various applications including gene expression profiling, DNA methylation analysis, genotyping, and others.
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