NGS data analysis Services

We provide comprehensive high-throughput data analysis services. Our bioinformatics offerings include standard as well as highly customized data analysis services along with biological interpretation as per the requirement. Our expertise includes but is not limited to the major NGS workflows for DNA, RNA and small RNA, metadata overlay, data mining, biological contextualization, and pathway analysis. All workflow steps include data type specific alignment and QC, coupled with powerful Genome Browser explorations to enable visual validations. Lead Sciences provides range of NGS Data Analysis services from different sequencing platform (illumina, 454, Ion-Torrent, PacBio, Nanopores etc) including

• Whole Genome sequence analysis
• Whole Exome sequence analysis
• De novo genome and transcriptome assembly
• Genome alignment and analysis
• Variant calling
• Visualization of genomics data
• Chip-Seq Analysis
• Methylome-Seq Analysis
• Reference Based RNA-Seq Analysis
• De-novo Based RNA-Seq Analysis
• MicroRNA-Seq Analysis
• Targeted re-sequencing (Exome-Seq) Analysis
• DNA-Seq (Genome variant Detection) Analysis
• Mapping, Annotation and Comparative Genomics Analysis (CGA)
• 16S / 28S / ITS rRNA Metagenomic Analysis
• Metatranscriptome Analysis