
Next generation sequencing (NGS) kits harness high-throughput techniques to answer a variety of genomic questions in many types of biological samples. NGS methods produce large amounts of data had have revolutionized genomic analysis; however a limiting factor is the ability to prepare samples with adequate throughput. The total sample preparation process can be divided into four areas: sample fragmentation, purification, enrichment, and library construction. With manual protocols these steps require significant manipulation and many hours of skilled genomic library production. Fully automated systems (post fragmentation), combine DNA library preparation and production into automated systems, at times producing sequence ready DNA libraries at a 5 times greater rate than manual methods.
Your search returned 55 NGS Kits across 1 supplier.
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- Twist Bovine Blocker Solution is a target enrichment reagent designed to improve sequencing efficiency. It has been ...
- Reactions = 2, 12
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- Versatile blockers compatible with multiple adapter types, minimizing nonspecific binding during target enrichment to ...
- Reactions = 2, 12, 96
- DNA Sequencing, NGS
- 1,536 full-length 10 bp UDI adapters enable high-throughput, PCR-free whole genome sequencing with efficient ...
- Samples = 96, 384
- DNA Sequencing
- 12 bp TruSeq-compatible adapters with 3,072 unique indexes for high-throughput, balanced NGS library prep—reducing...
- Plates = 96, Plate Format = 96x4, 384
- DNA Sequencing,RNA Sequencing, NGS
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- TruSeq-compatible methylated UMI adapters optimize cfDNA methylation studies by reducing false duplicates, preserving ...
- Samples = 96
- Whole Genome Sequencing, Oncology/Cancer Genomics
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- Twist's Synthetic human Mpox Virus (hMPXV) Controls are based on sequences from either the Congo Basin (CB) or West ...
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- The Twist Synthetic Respiratory Virus Controls cover a broad range of RNA and DNA viruses relevant to respiratory ...
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- NGS
- Twist's SARS-CoV-2 RNA Controls were created for several viral genomes, selected to cover a wide range of sequence ...
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- TruSeq-compatible UMI adapter system enabling accurate low-frequency variant detection from cfDNA and gDNA by reducing ...
- Samples = 96, 384
- DNA Sequencing,RNA Sequencing
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- TruSeq-compatible 10 bp adapters for all 'T-A' overhang workflows, preventing dimer formation and improving yield for ...
- Samples = 16, 96
- NGS
- Accelerate NGS library enrichment with hybridization times as short as 15 minutes in a streamlined, automatable workflow...
- Reactions = 2, 12, 96
- DNA Sequencing, NGS
- Rapid, one-hour hybridization workflow for Element sequencing, simplifying library enrichment while increasing ...
- Reactions = 12
- Epigenetics / Methylation(?), Low-frequency Variant ...
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- A specialized blocking reagent that increases the efficiency of targeted methylation sequencing by reducing off-target ...
- Reactions = 2, 12, 96
- DNA Sequencing
- Twist's original Standard Hybridization chemistry for efficient target capture with high uniformity, compatible with ...
- Reactions = 2, 12, 96
- DNA Sequencing
- Standard hybridization kit for efficient target capture with high uniformity, compatible with custom or catalog panels ...
- Reactions = 2, 12, 96
- DNA Sequencing
- Twist Dry Down Beads offer a streamlined approach to sample concentration by eliminating the need for a vacuum ...
- Reactions = 2, 12, 96
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- KEY BENEFITS
Exceptional, Consistent Performance
- Effective design, accurate synthesis, and detailed quality control ...
- EA
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- Target Enrichment
- Generate high-quality NGS libraries from low-input cfDNA or degraded samples in under two hours—ideal for liquid ...
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- DNA Sequencing, NGS
- NGS panel designed to provide high coverage uniformity that can integrate into any workflow
- kit contains reagents for 16 and 96 samples from singleplex ...
- Library preparation, Next-Generation Sequencing
- Target Enrichment
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- KEY BENEFITS More Complete Coverage • Adds 3.6 Mb of content to target all protein coding genes • Based on ...
- Available: 2 Reactions, 12 Reactions and 96 Reactions
- Next-Generation Sequencing; Whole Genome, Target Anylsis, ...
- Target Enrichment
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- KEY BENEFITS:
- Accommodate Either Enzymatic or Mechanical Fragmentation
- Use enzymatic fragmentation for automated, ...
- 16 Samples; 96 Samples
- Next-Generation Sequencing; Whole Genome, Target Anylsis, ...
- DNA Fragmentation
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- KEY BENEFITS: Accommodate Either Enzymatic or Mechanical Fragmentation • Use enzymatic fragmentation for automated...
- 16 Samples; 96 Samples
- Next-Generation Sequencing; Whole Genome, Target Anylsis, ...
- DNA Fragmentation, Adapter Ligation, Library Amplification
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- KEY BENEFITS Highly sensitive detection • Detection of as little as 10 copies of viral material with a fold ...
- Available: 2 Reactions, 12 Reactions and 96 Reactions
- Next-Generation Sequencing; Whole Genome, Target Anylsis, ...
- Target Enrichment
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- Comprehensive 41 Mb exome co-developed with CENTOGENE, combining rare disease insights and Twist technology for high-...
- Reactions = 2, 12, 96
- DNA Sequencing
- Targeted 72-gene panel co-developed with CENTOGENE, offering ≥99.5% coverage for detecting hereditary cancer ...
- Reactions = 2, 12, 96
- DNA Sequencing
- Curated 2,500-gene panel co-developed with CENTOGENE, offering ≥99.5% coverage for detecting variants in rare, ...
- Reactions = 2, 12, 96
- DNA Sequencing
- Comprehensive 40.5 Mb canine exome panel covering 17,000 genes, optimized for cancer and comparative genomics research ...
- Reactions = 2, 12, 96
- DNA Sequencing
- RNA-based fusion panel co-developed with CeGaT, targeting 160 genes across 30 cancers for sensitive, high-efficiency ...
- Reactions = 2, 12, 96
- DNA Sequencing
- Comprehensive exome panel co-developed with Broad Institute, offering high-uniformity coverage of coding and clinically ...
- Reactions = 2, 12, 96
- DNA Sequencing
- High-fidelity 20 Mb panel targeting 389 hard-to-sequence genes, improving coverage and variant detection in dark genomic...
- Reactions = 2, 12, 96
- DNA Sequencing
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