Long Non-Coding RNA Sequencing
Long non-coding RNAs (lncRNAs) are a large class of transcribed RNA molecules with a length of more than 200 nucleotides that do not encode proteins. Contact us today with any questions or for a no obligation quote.
Long Non-Coding RNA Sequencing Introduction
Long non-coding RNAs (lncRNAs) are thought to encompass nearly 30,000 different transcripts in humans, hence lncRNA transcripts account for the major part of the non-coding transcriptome. lncRNA discovery is still at an early stage and only a small proportion of lncRNAs have so far been investigated. Although we can start to classify different types of lncRNA functions, we are still far from being able to predict the function of new lncRNAs.
BGI Genomics offers expression profiling as one way to uncover the function of lncRNA. Identifying lncRNAs that are differentially expressed during development or in particular situations can shed light on their potential functions. Alternatively, looking for lncRNAs and protein-coding genes whose expression is correlated, can indicate co-regulation or related functions.
20 years of experience processing millions of RNA samples.
Precise quantification by UMI technology.
Rapid turnaround times and expert support, no project too big or small.
Long Non-Coding RNA Sequencing (lncRNA)-BGI Service Overview
Sample Requirements
Human / Mouse / Rat:
• Total RNA ≥ 200 ng
• Concentration ≥ 20 ng/μl
• General Quality Requirement: RIN ≥ 6.0
Sequencing Standards
• Guaranteed ≥85% of bases with quality score of ≥Q30
• ≥8 Gb sequencing data per sample is recommended.
Key Service Details
• Typical 27 working days from sample QC acceptance to filtered data availability
• Expedited services are available, contact us for more detail
• Reports and output data files are delivered in industry standard file formats: BAM, .xls, .png and FASTQ data.
Unique DNBSEQ™ Sequencing Technology
BGI Genomics' Long Non-Coding RNA Sequencing services are typically executed with proprietary DNBSEQ™ sequencing technology platforms, for great sequencing data at some of the lowest costs in the industry. DNBSEQ™ offers advantages in terms of lower amplification error rates and much lower duplication rates. In addition, studies have shown the lower index hopping rate in DNBSEQ™ platforms.
Contact us with any general enquiries or questions for our sequencing experts, we are here to help.
Access Further Sequencing Resources
We care for your samples from the start through to the result reporting. Highly experienced laboratory professionals follow strict quality procedures to ensure the integrity of your results. Access more sequencing resources below for full access to our range of educational resources and sample guides.
