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Sat & Sunday colsedMAIL US
info@allelelifesciences.comPHONE US
083770 82003
MON - FRI (9AM - 5PM)
Sat & Sunday colsedMAIL US
info@allelelifesciences.comPHONE US
083770 82003
Researchers and clinicians that need high-throughput sequencing capabilities for a variety of applications, including genomics, transcriptomics, metagenomics, and epigenomics, can easily access Next-Generation Sequencing (NGS) services. Usually, these services provide DNA or RNA sequencing to find genetic variants, gene expression levels, mutations, and more.
- Rapidly sequence whole genomes
- Epigenome Sequencing
- RNA Sequencing
- Sanger Sequencing
Primer sequencing, optimized PCR amplification, purification, and fragment analysis are services we offer. Affordable costs, quick turnaround, strict quality control, on-call tech support, and easy primer synthesis all contribute to the value of our service. We do our very best to ensure that every consumer has a reliable and positive experience.
Whole Genome Sequencing
Whole Exome Sequencing
De-novo Sequencing
Genotyping By Sequencing
The study of all epigenetic alterations in an organism, including modifications to its DNA and histones, is known as epigenomics.
Whole Genome Bisulfite Sequencing
Methylation Sequencing
Whole Genome Bisulfite Sequencing
5mC/5hmC Sequencing
MeDIP-Seq
ChIP-Seq
ATAC-Seq.
Transcriptomics is the high-throughput cataloging of all RNA transcripts, including non-coding and mRNA, in order to examine cellular gene expression under certain conditions. Using the precise and high-throughput next-generation sequencing method (NGS).
Single Cell RNA Sequencing
Small RNA Sequencing
Standard RNA Sequencing
Exosomal RNA Sequencing
CircRNA Sequencing.
Primer sequencing, optimized PCR amplification, purification, and fragment analysis are services we offer. Affordable costs, quick turnaround, strict quality control, on-call tech support, and easy primer synthesis all contribute to the value of our service..
Microbiome Analysis Services
PCR Sanger Sequencing.
