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sparQ DNA Frag & Library Prep Kit

Integrated enzymatic fragmentation and library prep with unrivaled speed and performance
Features & Benefits
  • High quality libraries in 2.5 hours from 1 ng – 1 μg of input DNA
  • Tunable and reproducible fragmentation size range
  • Simple, convenient 2-step workflow with minimal hands-on time
  • Novel chemistry and high-fidelity amplification minimizing bias
  • Superior sequence coverage uniformity and low duplication rate

 

sparQ DNA Frag & Library Prep Kit is intended for molecular biology applications. This product is not intended for the diagnosis, prevention or treatment of a disease.

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sparQ DNA Frag & Library Prep Kit
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Description

The sparQ DNA Frag & Library Prep Kit is optimized for enzymatic fragmentation of DNA and streamlined construction of high quality libraries for sequencing on Illumina NGS® platforms. The simple, convenient 2-step workflow can be completed in 2.5 hours with minimal hands-on time and accommodates DNA input amounts from 1 ng to 1000 ng. The DNA fragmentation and polishing reactions are combined in a single step to generate 5'-phosphorylated and 3'-dA-tailed fragments. This is followed by high efficiency adapter ligation in the same tube. PCR-Free workflows are enabled from 100 ng of starting material. If library amplification is required, the HiFi PCR Master Mix and Primer Mix ensure even amplification with minimal bias.


 

NGS Automation

Quantabio sparQ Frag & Library Prep Kit can be fully automated

Currently sparQ Frag & Library Prep Kit is supported by the following vendors:

Vendor Automation Platform(s)
PerkinElmer Applied Genomics SCICLONE G3 NGSx
Tecan DreamPrep® NGS
Beckman Coulter in development

 

Looking for more information or for different automation vendor?

Contact Us

 


 

sparQ UDI Adapter Resources

Setting up sparQ Library Prep kits in Illumina Experiment Manager

Featured Video

sparQ NGS Library Prep Solutions

 


 

What Customers Say
I have built >100 libraries with this kit and the results are great.
Genomics Core Director/Manager
West Virginia University

 

What Customers Say

The sparQ kit safeguards samples from over fragmentation and routinely provides more consistent fragment size. Once optimized, I had peace of mind knowing my samples were safe when I got busy in the lab.

Agricultural genomics institute
Scientist, Laboratory Manager
Details

Details

Contents

 

 

Volume

Component Description

Cap Color

24 Reactions

96 Reactions

DNA Frag & Polishing Enzyme Mix (5X)

Blue

1 x 240 µl

1 x 960 µl

DNA Frag & Polishing Buffer (10X)

Blue

1 x 120 µl

1 x 528 µl

DNA Frag & Polishing Enhancer Solution

Blue

1 x 288 µl

1 x 264 µl

DNA Ligase

Orange

1 x 240 µl

1 x 960 µl

DNA Rapid Ligation Buffer (5X)

Orange

1 x 480 µl

2 x 960 µl

HiFi PCR Master Mix (2X)

White

1 x 600 µl

2 x 1.2 ml

Primer Mix

White

1 x 72 µL

1 x 144 µl

Customer Testimonials

Customer Testimonials

sparQ DNA Frag & Library Prep Kit

“The sparQ kit safeguards samples from over fragmentation and routinely provides more consistent fragment size. Once optimized, I had peace of mind knowing my samples were safe when I got busy in the lab.”

Scientist, Laboratory Manager | Agricultural Genomics Institute
sparQ DNA Frag & Library Prep Kit

I have built >100 libraries with this kit and the results are great."

Genomics Core Director/ Manager | West Virginia University

Details

Contents

 

 

Volume

Component Description

Cap Color

24 Reactions

96 Reactions

DNA Frag & Polishing Enzyme Mix (5X)

Blue

1 x 240 µl

1 x 960 µl

DNA Frag & Polishing Buffer (10X)

Blue

1 x 120 µl

1 x 528 µl

DNA Frag & Polishing Enhancer Solution

Blue

1 x 288 µl

1 x 264 µl

DNA Ligase

Orange

1 x 240 µl

1 x 960 µl

DNA Rapid Ligation Buffer (5X)

Orange

1 x 480 µl

2 x 960 µl

HiFi PCR Master Mix (2X)

White

1 x 600 µl

2 x 1.2 ml

Primer Mix

White

1 x 72 µL

1 x 144 µl

Performance Data

Resources

Flyers

Product Manuals

Technical Notes

Brochures

CofA (PSFs)

SDSs

Publications

Altered costimulatory signals and hypoxia support chromatin landscapes limiting the functional potential of exhausted T cells in cancer
View ORCID ProfileB. Rhodes Ford - 2021
Abstract
Immunotherapy has changed cancer treatment with major clinical successes, but response rates remain low due in part to elevated prevalence of dysfunctional, terminally exhausted T cells. However, the mechanisms promoting progression to terminal exhaustion remain undefined. We profiled the histone modification landscape of tumor-infiltrating CD8 T cells throughout differentiation, finding terminally exhausted T cells possessed chromatin features limiting their transcriptional potential. Active enhancers enriched for bZIP/AP-1 transcription factor motifs lacked correlated gene expression, which were restored by immunotherapeutic costimulatory signaling. Epigenetic repression was also driven by an increase in histone bivalency, which we linked directly to hypoxia exposure. Our study is the first to profile the precise epigenetic changes during intratumoral differentiation to exhaustion, highlighting their altered function is driven by both improper costimulatory signals and environmental factors. These data suggest even terminally exhausted T cells remain poised for transcription in settings of increased costimulatory signaling and reduced hypoxia.
Comprehensive dataset of shotgun metagenomes from oxygen stratified freshwater lakes and ponds
Moritz Buck - 2021
Abstract
Stratified lakes and ponds featuring steep oxygen gradients are significant net sources of greenhouse gases and hotspots in the carbon cycle. Despite their significant biogeochemical roles, the microbial communities, especially in the oxygen depleted compartments, are poorly known. Here, we present a comprehensive dataset including 267 shotgun metagenomes from 41 stratified lakes and ponds mainly located in the boreal and subarctic regions, but also including one tropical reservoir and one temperate lake. For most lakes and ponds, the data includes a vertical sample set spanning from the oxic surface to the anoxic bottom layer. The majority of the samples were collected during the open water period, but also a total of 29 samples were collected from under the ice. In addition to the metagenomic sequences, the dataset includes environmental variables for the samples, such as oxygen, nutrient and organic carbon concentrations. The dataset is ideal for further exploring the microbial taxonomic and functional diversity in freshwater environments and potential climate change impacts on the functioning of these ecosystems.
Quantifying chromosomal instability from intratumoral karyotype diversity using agentbased modeling and Bayesian inference
A.R. Lynch - 2021
Abstract
Chromosomal instability (CIN) — persistent chromosome gain or loss through abnormal karyokinesis — is a hallmark of cancer that drives aneuploidy. Intrinsic chromosome mis-segregation rates, a measure of CIN, can inform prognosis and are a likely biomarker for response to anti-microtubule agents. However, existing methodologies to measure this rate are labor intensive, indirect, and confounded by karyotype selection reducing observable diversity. We developed a framework to simulate and measure CIN, accounting for karyotype selection, and recapitulated karyotype-level clonality in simulated populations. We leveraged approximate Bayesian computation using phylogenetic topology and diversity to infer mis-segregation rates and karyotype selection from single-cell DNA sequencing data. Experimental validation of this approach revealed extensive chromosome mis-segregation rates caused by the chemotherapy paclitaxel (17.5±0.14/division). Extending this approach to clinical samples revealed the inferred rates fell within direct observations of cancer cell lines. This work provides the necessary framework to quantify CIN in human tumors and develop it as a predictive biomarker.
Monodopsis and Vischeria Genomes Shed New Light on the Biology of Eustigmatophyte Algae
Hsiao-Pei Yang - 2021
Abstract
Members of eustigmatophyte algae, especially Nannochloropsis and Microchloropsis, have been tapped for biofuel production owing to their exceptionally high lipid content. Although extensive genomic, transcriptomic, and synthetic biology toolkits have been made available for Nannochloropsis andMicrochloropsis, very little is known about other eustigmatophytes. Herewe present three near-chromosomal and gapless genome assemblies of Monodopsis strains C73 and C141 (60Mb) and Vischeria strain C74 (106Mb), which are the sister groups to Nannochloropsis andMicrochloropsis in the order Eustigmatales. These genomes contain unusually high percentages of simple repeats, ranging from 12% to 21% of the total assembly size. Unlike Nannochloropsis and Microchloropsis, long interspersed nuclear element repeats are abundant in Monodopsis and Vischeria and might constitute the centromeric regions. We found that both mevalonate and nonmevalonate pathways for terpenoid biosynthesis are present in Monodopsis and Vischeria, which is different from Nannochloropsis and Microchloropsis that have only the latter. Our analysis further revealed extensive spliced leader trans-splicing in Monodopsis and Vischeria at 36–61% of genes. Altogether, the highquality genomes of Monodopsis and Vischeria not only serve as the much-needed outgroups to advance Nannochloropsis and Microchloropsis research, but also shed new light on the biology and evolution of eustigmatophyte algae.
Optimization of Enzymatic Fragmentation is Crucial To Maximize Genome Coverage: A Comparison of Library Preparation Methods for Illumina Sequencing
Teodora Ribarska - 2021
Abstract
Background Novel commercial kits for whole genome library preparation for next-generation sequencing on Illumina platforms promise shorter workflows, lower inputs and cost savings. Time savings are achieved by employing enzymatic DNA fragmentation and by combining end-repair and tailing reactions. Fewer cleanup steps also allow greater DNA input flexibility (1 ng-1 μg), PCR-free options from 100 ng DNA, and lower price as compared to the well-established sonication and tagmentation-based DNA library preparation kits. Results We compared the performance of four enzymatic fragmentation-based DNA library preparation kits (from New England Biolabs, Roche, Swift Biosciences and Quantabio) to a tagmentation-based kit (Illumina) using low input DNA amounts (10 ng) and PCR-free reactions with 100 ng DNA. With four technical replicates of each input amount and kit, we compared the kits` fragmentation sequence-bias as well as performance parameters such as sequence coverage and the clinically relevant detection of single nucleotide and indel variants. While all kits produced high quality sequence data and demonstrated similar performance, several enzymatic fragmentation methods produced library insert sizes which deviated from those intended. Libraries with longer insert lengths performed better in terms of coverage, SNV and indel detection. Lower performance of shorter-insert libraries could be explained by loss of sequence coverage to overlapping paired-end reads, exacerbated by the preferential sequencing of shorter fragments on Illumina sequencers. We also observed that libraries prepared with minimal or no PCR performed best with regard to indel detection. Conclusions The enzymatic fragmentation-based DNA library preparation kits from NEB, Roche, Swift and Quantabio are good alternatives to the tagmentation based Nextera DNA flex kit from Illumina, offering reproducible results using flexible DNA inputs, quick workflows and lower prices. Libraries with insert DNA fragments longer than the cumulative sum of both read lengths avoid read overlap, thus produce more informative data that leads to strongly improved genome coverage and consequently also increased sensitivity and precision of SNP and indel detection. In order to best utilize such enzymatic fragmentation reagents, researchers should be prepared to invest time to optimize fragmentation conditions for their particular samples. Background During the last decade, Illumina technology has come to dominate short read next generation sequencing, offering cost-effective high precision data for a wide variety of applications such as whole genome sequencing (WGS), metagenomics and transcriptomics. In medical genetics, WGS is increasingly applied to identify disease-causing genetic variation (SNPs or structural variants), disease susceptibility, cancer evolution and drug response, among a plethora of other applications (1–3). Since the cost of next generation sequencing is still high and often the amount of available DNA from the biological source is limited, methodological efforts are constantly underway to improve the efficiency of WGS, i.e. extracting the most unique genetic information, with the highest possible quality and coverage, from a variety of input DNA amounts and qualities, at the lowest cost and shortest hands-on time. Library preparation is an essential process preceding sequencing itself, and comprises several aspects that affect the efficiency of WGS. It typically involves the following main steps: fragmentation of the input DNA, end-repair and A-tailing of the DNA fragments, ligation of indexed sequencing adapters and optional amplification of the ligated products. In addition, one or more cleanup steps are necessary in between steps to purify the DNA reaction products of reagents from the previous reaction. The most commonly used methods for fragmentation of genomic DNA are sonication, tagmentation (i.e., transposition of partial adapters into the DNA), and enzymatic digestion by DNA endonucleases. Prior to the widespread adoption of enzymatic fragmentation, sonication was preferred, as it produces nearrandom fragmentation, and fragment length can be adjusted by varying sonication time and strength. However, this requires a DNA sonication instrument and in some cases also special consumable sonication tubes, adding considerable cost and handling time to the procedure. Based on sonication, Illumina s tagmentation based Nextera reagents, albeit not allowing PCR-free prep (until recently, in its renamed version Illumina DNA prep). The principle of tagmentation is the insertion by transposition of partial sequencing adapter sequences in genomic DNA that in effect fragments and adds adapters in a single step. Subsequently, the adapters are extended to full length by PCR (in the Nextera DNA flex kit) and through an undisclosed PCR-free method in the Illumina DNA PCR-free kit. The length of the DNA between the transposed adapters is dependent on the size of the beads and the concentration of the transposomes (transposase loaded with adapters) coating on them(4), which is fixed for the respective kit. The sole possibility to modulate this length is by means of size selection after library preparation is complete, which may discard a considerable portion of the library. In recent years many competitor library prep kits that use enzymatic fragmentation have emerged. Offering quick and simple workflows, high flexibility of DNA input amounts, PCR-free options with approximately 100 ng DNA, and importantly a lower price, these kits offer attractive alternatives. Here, we compare the performance of several of these kits. In order to evaluate the performance and sequencing data quality produced with enzymatic fragmentation-based library prep kits, we performed WGS using four such kits (from New England Biolabs, Quantabio, Swift Biosciences and Roche) and the Nextera DNA flex tagmentation based kit (from Illumina) with 10 Page 3/9 and 100 ng DNA inputs, and sequenced them on an Illumina HiSeq X instrument. All of the tested kits reproducibly delivered similar high-quality data in terms of coverage and precision of single nucleotide variant (SNV) and indel detection. We observed that libraries with DNA insert size longer than the combined sequencing reads length exhibited improved performance than those with shorter length. However, there is an optimum insert length, beyond which further increase in insert length does not augment the sequencing data performance but can reduce clustering efficiency and data yields. Results Study design We compared the WGS performance of four enzymatic fragmentation-based library preparation kits: NEBNext Ultra II FS from NEB (hereafter referred to as NEB), Swift 2S Turbo flexible from Swift Biosciences (hereafter Swift2S), SparQ DNA Frag and Library Prep from Quantabio (Quanta) and KAPA HyperPlus from Roche (Kapa) with the tagmentation-based Nextera DNA FLEX kit from Illumina (Nextera). In our study design we prepared libraries from 10 ng and 100 ng input DNA amounts, whereby the 100 ng input reactions were PCR-free (or with minimal PCR cycles, where absolutely required; see Table 1 for details). An entirely PCR-free option was not possible for Nextera and NEB kits, in which PCR is necessary to complete the sequencing adapters (and add indexes). With four technical replicates for each input amount and kit, we aimed to test the reproducibility and robustness of the kits, with respect to fragment size distribution and quality of the sequencing data. As input DNA we used genomic DNA from the human fibroblast cell line NA12878 (purchased from Coriell Institute) that has been well characterized (e.g. for indels and single nucleotide variants) and often used as standard control DNA source for genomic studiescalled therefore also “genome in a bottle” (5, 6). Library concentrations produced by each replicate are summarized in Additional Table 1. The libraries from 10 and 100 ng DNA inputs, each in four technical replicates, were pooled and sequenced over 20 lanes of HiSeq X flowcells (i.e. four lanes per kit), with 150 bp paired end reads.
Microbial mitigation of greenhouse gas emissions from boreal lakes
Gaëtan Martin - 2021
Abstract
The climate change crisis has drawn the attention of both the public and scientific community to the carbon cycle and particularly to the importance of greenhouse gases (GHG) carbon dioxide (CO2) and methane (CH4). CO2 has been a key component of Earth´s climate regulation throughout its geological history and is now the main driver of the current change in climate. CH4 has been responsible for a quarter of the cumulative radiative forcing observed so far. Recent studies suggest that lakes could be a major source of both CO2 and CH4. Boreal lakes are of special interest as they represent 27% of the global lake area, and their production of CO2 and CH4 are expected to increase in the future. This project aimed to investigate microbial processes with the potential to limit the emissions of GHGs from boreal lakes. For that purpose, the impact of an increase in phosphorus (P) concentration in the water on CH4 oxidation under the ice was investigated as well as the community composition of the methanotrophic guild. We also looked at the potential importance of chemolithoautotrophic microorganisms in fixing CO2 in the water column. Using a combination of geochemical analysis, genomic studies, and in vivo assays, we showed that P amendment has the potential to increase methane oxidation, possibly limiting the expected increase in CH4 emissions due to anthropogenic fertilization of boreal lakes. We also showed that methanotrophic community structure in boreal lakes is driven by CH4 concentration and that alphaproteobacterial methanotrophs might play an important role in removing CH4 from surface waters. Finally, we showed that dark carbon fixation is a common trait in boreal lakes and that it seems related to the iron cycle.
Comprehensive dataset of shotgun metagenomes from stratified freshwater lakes and ponds
Moritz Buck - 2020
Abstract
Stratified lakes and ponds featuring steep oxygen gradients are significant net sources of greenhouse gases and hotspots in the carbon cycle. Despite their significant biogeochemical roles, the microbial communities, especially in the oxygen depleted compartments, are poorly known. Here, we present a comprehensive dataset including 267 shotgun metagenomes from 41 stratified lakes and ponds mainly located in the boreal and subarctic regions, but also including one tropical reservoir and one temperate lake. For most lakes and ponds, the data includes a vertical sample set spanning from the oxic surface to the anoxic bottom layer. The majority of the samples were collected during the open water period, but also a total of 29 samples were collected from under the ice. In addition to the metagenomic sequences, the dataset includes environmental variables for the samples, such as oxygen, nutrient and organic carbon concentrations. The dataset is ideal for further exploring the microbial taxonomic and functional diversity in freshwater environments and potential climate change impacts on the functioning of these ecosystems.
ISSRseq: an extensible, low-cost, and efficient method for reduced representation sequencing
Brandon T. Sinn - 2020
Abstract
1. The capability to generate densely sampled single nucleotide polymorphism (SNP) data is essential in diverse subdisciplines of biology, including crop breeding, pathology, forensics, forestry, ecology, evolution, and conservation. However, access to the expensive equipment and bioinformatics infrastructure required for genome-scale sequencing is still a limiting factor in the developing world and for institutions with limited resources. 2. Here we present ISSRseq, a PCR-based method for reduced representation of genomic variation using simple sequence repeats as priming sites to sequence inter-simple sequence repeat (ISSR) regions. Briefly, ISSR regions are amplified with single primers, pooled, and used to construct sequencing libraries with a low-cost, efficient commercial kit, and sequenced on the Illumina platform. We also present a flexible bioinformatic pipeline that assembles ISSR loci, calls and hard filters variants, outputs data matrices in common formats, and conducts population analyses using R. 3. Using three angiosperm species as case studies, we demonstrate that ISSRseq is highly repeatable, necessitates only simple wet-lab skills and commonplace instrumentation, is flexible in terms of the number of single primers used, is low-cost, and can generate genomic-scale variant discovery on par with existing RRS methods that require high sample integrity and concentration. 4. ISSRseq represents a straightforward approach to SNP genotyping in any organism, and we predict that this method will be particularly useful for those studying population genomics and phylogeography of non-model organisms. Furthermore, the ease of ISSRseq relative to other RRS methods should prove useful for those conducting research in undergraduate and graduate environments, and more broadly by those lacking access to expensive instrumentation or expertise in bioinformatics.
Complete Genomes of Symbiotic Cyanobacteria Clarify the Evolution of Vanadium-Nitrogenase
Jessica M. Nelson - 2019
Abstract
Plant endosymbiosis with nitrogen-fixing cyanobacteria has independently evolved in diverse plant lineages, offering a unique window to study the evolution and genetics of plant–microbe interaction. However, very few complete genomes exist for plant cyanobionts, and therefore little is known about their genomic and functional diversity. Here, we present four complete genomes of cyanobacteria isolated from bryophytes. Nanopore long-read sequencing allowed us to obtain circular contigs for all the main chromosomes and most of the plasmids. We found that despite having a low 16S rRNA sequence divergence, the four isolates exhibit considerable genome reorganizations and variation in gene content. Furthermore, three of the four isolates possess genes encoding vanadium (V)-nitrogenase (vnf), which is uncommon among diazotrophs and has not been previously reported in plant cyanobionts. In two cases, the vnf genes were found on plasmids, implying possible plasmid-mediated horizontal gene transfers. Comparative genomic analysis of vnf-containing cyanobacteria further identified a conserved gene cluster. Many genes in this cluster have not been functionally characterized and would be promising candidates for future studies to elucidate V-nitrogenase function and regulation.
Click here to see all Publications

Customer Testimonials

sparQ DNA Frag & Library Prep Kit

“The sparQ kit safeguards samples from over fragmentation and routinely provides more consistent fragment size. Once optimized, I had peace of mind knowing my samples were safe when I got busy in the lab.”

Scientist, Laboratory Manager | Agricultural Genomics Institute
sparQ DNA Frag & Library Prep Kit

I have built >100 libraries with this kit and the results are great."

Genomics Core Director/ Manager | West Virginia University

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