NGS(DNA/RNA-Seq)

We provide whole genome sequencing service from gDNA samples using NGS technology. We report SNP, INDEL, CNV, Structural variation data and others

Sample requirement	>2ug gDNA
Library method	Illumina TruSeq Nano DNA Library kit
NGS run format	NovaSeq 6000, PE150
Data yield	~90 Gb/sample
Turnaround time	~7 weeks after DNA QC
Sample type	gDNA

++ If you want to get DNA prep.service, you can send us your samples after discussing with us.

SNP(Single Nucleotide Polymorphism), INDEL (Insertion & Deletion), CNV(Copy Number Variation), Structural Variation analysis and Others

Whole Exome Sequencing is a method of analyzing genes in the Exom area by creating a library by selectively capturing only Exon areas. We report SNP, INDEL, CNV, Structural variation data and others

Sample requirement	>2ug gDNA
Library method	Agilent SureSelect kit
NGS run format	NovaSeq 6000, PE100
Data yield	~6 Gb (100X depth)/sample
Turnaround time	~6 weeks after DNA QC
Sample type	gDNA

++ If you want to get DNA prep.service, you can send us your samples after discussing with us.

SNP(Single Nucleotide Polymorphism), INDEL (Insertion & Deletion), CNV(Copy Number Variation), Structural Variation analysis and Others

Enzymatic Methyl-Seq(EM-Seq) is DNA methylation experiment and data analysis service without DNA damage. This provide researcher with high qualified data because EM-Seq efficiently detects 5-mC and 5-hmC using enzyme-based method as compared with Whole Genome Bisulfite Sequencing(WGBS) using bisulfite conversion method.

Sample requirement	>2ug gDNA
Library method	NEBNextⓇ Enzymatic Mehyl-seq kit
NGS run format	Illumina NovaSeq6000, PE150bp
Data yield	~120G/sample
Turnaround time	~6 weeks after DNA QC
Sample type	gDNA

We support various analysis such as ExPADA Report, Methylation Calling, Differential Methylated Cytosines(DMC) Analysis & Annotation, Differential Methylated Regions(DMR) Analysis & Annotation, Sample Correlation & PCA plot et cetera..

We provide considerably useful ChIP-Seq service for epigenetics study that analyzes the interaction of DNA and regulatory protein. With professional experiment know-hows and analysis technique developed over a long period of time, we provide data that meet the needs of a researcher.

Sample requirement	>20ul IP-DNA
Library method	NEB Ultra DNA Library kit
NGS run format	Illumina NovaSeq6000, PE100bp
Data yield	~4G/sample
Turnaround time	~3 weeks after Library QC
Sample type	IP-DNA

We support various analysis such as ExDEGA Report, Peak Annotation, Motif Discovery, Tags Comparison, IGV, BedGraph, Data Mining et cetera..

ATAC-seq (Assay for Transposase-Accessible Chromatin using sequencing) is a technique used in molecular biology to assess genome-wide chromatin accessibility. ATAC-seq identifies accessible DNA regions by probing open chromatin with hyperactive mutant Tn5 Transposase that inserts sequencing adapters into open regions of the genome.

Sample requirement	>~1x106 cells in 1ml media (Cell viability >80%)
Library method	ACTIVE MOTIF® ATAC-Seq Kit
NGS run format	NovaSeq 6000, PE100
Data yield	~6G/ sample
Turnaround time	~5 weeks after Cell QC
Sample type	Cell

We support various analysis such as ExPADA Report, Peak Annotation, Motif Discovery, Tags Comparison, IGV, BedGraph, Data Mining et cetera.

Provides metagenomic and microbiome analysis which identifies and quantifies microbial community (bacteria, fungi, etc) derived from various environments including soil, air, water, and human body by using 16s rRNA sequencing.

Sample requirement	>0.1 ng/ul gDNA
Library method	16S rRNA Amplicon Library for illumina
NGS run format	Illumina MiSeq, PE300bp(Paired End 300bp)
Data yield	~50,000 reads/sample
Turnaround time	~4 weeks after Library QC
Sample type	gDNA

++ If you want to get DNA prep.service, you can send us your samples after discussing with us.

We support various analysis such as Assembly Result, Feature Table, Taxonomy(Bar & Pie Chart, Profile Data), Diversity(Alpha, Beta), Sample Clustering et cetera.