NGS Data Analysis Services

Bioinformatics analysis of sequencing data ranges from processing sequencing reads from an sequencing machine to data analysis and deep mining of data across multiple sample types. Data analysis can be of three broad stages of primary, secondary and tertiary analysis. Whether you just want to have your sequence data analyzed or need help setting up a custom reproducible analysis pipeline or custom scripts or publication type if figures/tables we are highly industry expert to deliver all custom based services.We provide services to global and Arraygen is first choice for all researchers with the quality report.We provide NGS custom data Analysis for all platform illumina,ion torrent,Long reads pacbio and nanopore.We work with all kingdom either Eukaryote/Prokaryote/Archaea.
NGS Data Analysis Services Description Price
Reference Based RNASeq We use highly robust statistical models to identify differentially expressed genes (DEG) from raw RNA-Seq data. All list of DEG Up and Down along with GO and pathway enrichment and different plots heatmap, Volcano. We also help you assess data quality and verify your experimental design with all undersatnding of your analysis as well as different differential Expression tool EdgeR or DESEQ2 or Cuffdiff can be used as per your requirement. Enquire
Denovo Based RNASeq We use highly robust statistical models to identify differentially expressed genes (DEG) from raw RNA-Seq data. transcriptome assembly and validation will be made using trinity. All list of DEG Up and Down along with GO and pathway enrichment and different plots heatmap, Volcano. We also help you assess data quality and verify your experimental design with all undersatnding of your analysis as well as different differential Expression tool EdgeR or DESEQ2 or Cuffdiff can be used as per your requirement. Enquire
DNASeq - Variation Calling We use highly robust statistical models to identify potential mutations either SNP / Inerstions / Deletions / CNVs from whole genome or whole exome data. We are expert to provide variations annotations as well as list of few potential variations which can be potential markers to identify disease cause. We have provided whole exome automated pipeline recently to epigeneres cancer study company. Enquire
ChipSeq - DNA-Protein Binding We use highly robust statistical models to identify DNA- protein binding regions from whole genome data. We are expert to provide peak regions / annotations to upstream / downstream as well as potential motifs involved in the region. Enquire
Targeted Metagenomics Targeted metagenome analysis we provide eith 16s rRNA or 18s RNA or ITS regions and species detected. We use qiime2 pipeline to make more standered report and all results provided as per the publication standerds. Enquire
Whole Genome Metagenome We are highly expertise with whole genome metagenome analysis and we use different tools like squeezmeta and bining process as well as bin vizualization using anvio. We also integrate post analysis with sqmtools for making highly interactive plots like krona / stacked bar plot / heatmap abundance plot. All the results are provided ready to use. We also accept client request as needed publication standered for tables / figures. Enquire
DNA Methylation DNA methylation analysis like RRBS methods as well as all analysis report using bismark and methylkit. Differential methylated reports and hypo as well as hyper methylated regions along with annotation. Enquire
Single Cell RNASeq We are highly expertise in SCRNAseq data analysis and cell ranger tool is used to preprocess raw data and seurat as well as highly specilized in house python scripts have been developed. We deliver high interactive plots and advanced QC matrics and Interactive tSNE plots with cell type and cluster information as well as heatmap vizualization. Enquire
LncRNASeq We use highly expertise in detecting LncRNA as well as filter only non code RNAs and removal of all coding potential RNAs. Enquire
miRNASeq We use highly robust statistical models to identify differentially expressed miRNAs (DEG) from raw RNA-Seq data(Known and novel miRNAs). All list of DEG Up and Down along with target genes with GO and pathway enrichment and different plots heatmap, Volcano. We also help you assess data quality and verify your experimental design with all undersatnding of your analysis as well as different differential Expression tool EdgeR or DESEQ2 can be used as per your requirement. Enquire
ATASeq We use highly expertise in analysing ATASeq data. We are expert to provide peak regions / annotations to upstream / downstream as well as potential motifs involved in the region. Enquire
CRISPR Data Analysis We are highly experts in designing sgRNA as well as data analysis for crispr edited regions. Reports with variations for offsite or onsite along with annotation is reported. Enquire
NGS Automated Pipeline Development We are highly expertise in making any NGS data analysis from raw data to reports in one click with automated scripts based on python scripts. Enquire
NGS Genomics Database Development We are highly expertise in genomics database development either stand alone GUI software or command line based. Enquire
Circos Genome Representation We are highly expertise in generating advanced circular genome vizualziations using circos tools. Enquire
TCGA Data Analysis We can analyze data from TCGA for any cancer type and further provide statistically analyzed results. Enquire
Genome Annotation We are highly expertise for the genome / transcriptome annotation either for plant or any eukaryotes or any prokaryotes. Enquire
Metatranscriptome Data Analysis We use highly robust statistical models to identify differentially expressed genes (DEG) from raw metatranscriptomic/metabolomics data. All list of DEG Up and Down along with GO and pathway enrichment and different plots heatmap, Volcano. We also help you assess data quality and verify your experimental design with all undersatnding of your analysis as well as different differential Expression tool EdgeR or DESEQ2 can be used as per your requirement. We also use metaphyln or Humann for advance analysis. Enquire
Custom Data Analysis We provide any custom data analysis for any NGS applications / microarray / genomics / bioinformatics. We are expertise in development of algorithms for any NGS application(automated scripts) as well as database development. We have recently developed automated python scripts for epegeneres biotech company for transcriptome as well as whole exome. We developed database only for cancer study based on variations and expression data for epigeneres. Enquire