Library Preparation

We provide library preparation services for many sample types and applications for the Illumina sequencing platforms. 

Please download our full services and fees description here.  To request a pricing quote or instructions to prepare a sample for sequencing, please email ntgcresearch@uta.edu

DNA Library Preparation

All DNA library preparation processing will undergo quality control (QC) to make sure it is of high enough quality and quantity. The QC of each sample includes Qubit for concentration (ng/ul) and agarose gel electrophoresis to check quality.  The cost of the QC is included in the price of library preparation. If a sample fails QC, the user will be charged for the QC portion only.

DNA Library Preparation KitDescriptionTypical Run Type
Illumina TruSeq DNA PCR FreeWGS of small genomes and whole-human genome sequencingNovaSeq 6000 2x150bp
Nextera XT DNAPrepare libraries for small genomes, PCR amplicons and plasmids to sequence using MiSeq technology; Multiplex up to 384 samplesNovaSeq 6000 2x150bp
Nextera Rapid Capture ExomeAll-in-one kit for library preparation and exome enrichment (100X coverage = 80M paired reads per sample)NovaSeq 6000 2x150bp
TruSeq Exome/TruSeq Rapid ExomeAll-in-one kit for library preparation and exome enrichment; includes 45Mb of exonic content; up to 12 unique indexes; TruSeq Exome is FFPE compatibleNovaSeq 6000 2x75bp
16S Metagenomics (rRNA Sequencing)Amplicon sequencing method used to identify and compare bacteria present within a given sample; primer pair sequences for the V3 and V4 region that create a single amplicon of approximately ~460bp (~100,000 reads per sample)MiSeq v3 2x250bp
Illumina TruSeq Custom Amplicon KitPool up to 96 samples for maximum benefit from the MiSeq v3 reagents; access automated, design-specific variant calling and final data analysis using the Illumina MiSeq software; FFPE DNA compatibleWe work with an Illumina Sales Representative to order a custom project.

Total RNA-seq Library Preparation

Whole-transcriptome analysis with total RNA sequencing (RNA-Seq) detects coding plus multiple forms of noncoding RNA. Total RNA-Seq can accurately measure gene and transcript abundance and identify known and novel features of the transcriptome.

RNA Library Preparation KitDescriptionTypical Run Type
Illumina TruSeq Stranded Total RNA with Ribo Zero GoldWhole-transcriptome analysisNovaSeq 1x75bp, 2x75bp or 2x150bp

NGS Samples for Library Preparation Submission

Below are the quantity and volume needed for sample submission depending on which services you request.  Submit samples in 1.5 ml Lo-bind microfuge tubes, labeled clearly with order number, submission date and sample identity.  

Please quantify the DNA and RNA concentrations using fluorometry. Sample quantification is required prior to submission.

Library TypesMinimum QuantityA260/280RNA Integrity (RIN)Concentration (per Qubit)Shipment Method
RNA-Seq Samples5 ug>1.8-2.0>7.0~100 ng/uldry ice
mRNA Sequencing5 ug>1.8-2.0>7.0~100 ng/uldry ice
Whole Transcriptome2 ug>1.8-2.0>7.0~100 ng/uldry ice
Illumina Small RNA Seq2 ug>1.8-2.0>7.0~200 ng/uldry ice
ChIP-Seq Samples (DNA should be sheared to 200-600 bp)5 ng for the ChIP DNA sample (50 ng for the input DNA sample)dry ice
Exome Sequencing1-5 ug~100 ng/uldry ice
Whole Genome Sequencing2 ug>1.8-2.0>20 ng/uldry ice
16S Metagenomic Samples20 ng>5 ng/uldry ice

Prepared Libraries for Submission

All clients are responsible for their own QC (quantification and fragment analysis) and library pooling prior to submission.

NovaSeq 6000StandardXP Workflow (per lane)
SP/S14nM at 110uL4nM at 25uL
S24nM at 165uL4nM at 30uL
S44nM at 325uL4nM at 40uL
iSeqSP/S1, S2, S44nM at 25uL
MiSeqSP/S1, S2, S44nM at 25uL

Questions?

We are here to help!  Please contact us!