Reason #4: Wide range of bioinformatics and data modeling solutions that we cover
Our bioinformaticians develop and implement solutions for researchers across a variety of research domains, working with 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, and even research projects focusing on microbial and viral species.
The types of projects we carry out include: processing, analyzing, and interpreting high-throughput biological and medical data, with a focus on next-generation sequencing (NGS) data, genomics, transcriptomics, proteomics, metabolomics, and other omics data. We also offer statistical data analysis and data integration for diverse biomedical and other data types, helping to identify causal relationships or other hidden information between measured variables. In addition, we offer AI/machine learning/deep learning modeling, structural bioinformatics (such as AlphaFold and I-TASSER modeling), metagenomics, ecology, phylogenetics, population genetics, and other analyses related to evolutionary biology. We also provide customized and advanced analysis method development, specific data structure and algorithm development, informatics, database development and maintenance, software solutions, and even IT and infrastructure solutions.
Our team is experienced in handling next-generation sequencing (NGS) data from all common platforms, including Illumina, Ion Torrent, Pacific Biosciences (PacBio) and Oxford Nanopore Technologies (ONT). We have expertise in all common NGS applications, including whole-genome sequencing (mapping-based or assembly-based approaches), exome and other targeted sequencing, bulk RNA-seq, single-cell RNA-seq, ChIP-seq for transcription factors, RNA PolII and histone modifications, ATAC-seq, CUT&RUN, CUT&Tag, HiChip, PLAC-seq, Multiome, and various sequencing-based DNA methylation applications. We are also skilled in less frequently used NGS applications such as DNase-seq, CLIP-seq, 4C-seq, Hi-C, ChIA-PET, and immunosequencing. Additionally, we are capable of assisting in developing novel NGS applications.
Read this blog page to learn more about the Illumina, PacBio, and Oxford Nanopore technologies and which one might be best for your project.
Read this blog page to learn about scRNA-seq, scATAC, and Multiome, as well as the bioinformatics analysis procedures for these single-cell analysis protocols.
Read this blog series for a discussion on AlphaFold 2 modeling, the strengths of AlphaFold 2, and how to run it.
We are able to handle microarray data from all major platforms, including Affymetrix, Agilent, Illumina, and NimbleGen, for various applications such as gene expression profiling, DNA methylation analysis, genotyping, and others.
We have experience in developing AI/deep learning/deep neural network-based models in the biological/biomedical domains (read our blog series here).
Want to know why we can handle so many different types of bioinformatics solutions? See the discussion on the experiences of our Lead Bioinformaticians (LBs) at this page. See a discussion on the guarantee we offer at this page, and how we assist in manuscript reviews here.
Other Reasons Why You Should Use AccuraScience's Services