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REPLI-g Single Cell RNA Library Kit
For RNA library construction from single cells for Illumina sequencing applications 
    • MDA-based, PCR-free single cell library construction
    • Comprehensive and accurate transcriptome profiling of single cells
    • Fast time-to-result through a streamlined protocol
    • Minimal bias and sensitive detection of low-abundance transcripts
    • High-quality libraries, ready for use on any Illumina NGS platform
GeneRead qPCR SYBR® Green Mastermix
For use with the GeneRead Library Quant System
    • Specific products with minimal primer–dimers
    • Instrument-specific all-in-one mixes
    • Available with ROX or fluorescein
Generation DNA Purif. Solution

Generation Capture Kitを用いたゲノムDNA精製に使用

    • 迅速かつ簡単な操作手順
    • 標準的なPCRスクリーニングなどのアプリケーションに最適
    • 精製したDNAは標準的なPCRに直ちに使用可能
GeneRead DNAseq Panel PCR Kit V2
ターゲットエンリッチメントのためのGeneRead DNAseq Panles V2用PCRキット
    • 高い特異性と均質性
    • GeneRead DNAseq Panels V2との併用に最適化
GeneRead DNAseq Library Quant Array
For qPCR-enabled quantification of NGS libraries before sequencing
    • Predispensed sequentially diluted DNA standard; no manual titration
    • Quality score enables removal of low-quality libraries before sequencing
    • Data analysis Excel sheet automatically calculates library concentration
    • Simple protocol, high sensitivity, and wide dynamic range
    • Compatible with all major NGS platforms and qPCR instruments
QIAseq and GeneRead Library Prep Kits
NGSアプリケーションのための、迅速で効率の良いDNAライブラリー調製
    • 1本のチューブを用いた迅速な手法により最大50%まで時間を短縮
    • 少量のスタートサンプルで高い収量
    • オプションのハイフィデリティ増幅ステップで配列に偏りのない増幅
    • マルチプレックス、ハイスループット処理が可能
GeneRead Size Selection Kit
NGSライブラリー調製用の迅速で信頼できる150 bp以下のDNAフラグメントの除去
    • DNA フラグメントの正確なサイズ選択
    • QIAGEN の実証済みのシリカカラムテクノロジーをベースにした迅速な操作
    • QIAcube上で自動化可能な分かりやすいプロトコール
GeneRead DNA FFPE Kit
信頼性の高いNGS 解析を実現するためのFFPE 組織からのgDNA 分離
    • FFPE サンプルからの最適化されたgDNA 精製
    • シトシンの脱アミノ化によるアーティファクトを酵素により除去
    • false SNP callのリスクを最小化
    • DNAシークエンシングアプリケーションで卓越した結果
    • QIAcubeで自動化可能
GeneRead DNAseq Custom Panel V2
ヒト遺伝子またはゲノム領域に対応するカスタマイズ可能なターゲットエンリッチメント
    • 優れたシークエンシングパフォーマンス
    • 必要なDNA量はたった10 ng/チューブ
    • FFPEサンプルを含む多様なサンプルに対応
    • 主要なNGSプラットフォームに対応
    • ヒトゲノム遺伝子上の任意の遺伝子、ゲノム領域からのカスタマイズに対応
GeneRead DNA Library Q Kit
Automated and streamlined to save time
    • Affordable automation reducing hands-on time by up to 75%
    • Minimal input material of only 4ng needed
    • Experimentally verified with the entire Sample-to-Insight GeneReader NGS workflow
    • Can be paired with the QIAxcel for size-determination to further reduce hand-on time
GeneRead QIAact Panels, Powered by QCI
実用的な知見が得られるパネル
    • GeneRead QIAact Panel ファミリーの第一弾
    • 研究に関連性が最も高い遺伝子および変異を精査したデザイン
    • GeneReader NGS System で実証済みのパフォーマンス
    • FFPE サンプル由来のDNA を用いて検証済み
GeneRead Clonal Amp Q Kit
For clonal amplification of DNA libraries for next-generation sequencing (NGS) ...
    • Generation of sequencing-ready amplified libraries
    • Multiplex clonal amplification: each library pool can include up to 12 uniquely bar coded DNA library samples
    • Automated on the GeneRead QIAcube
    • Proven performance with the GeneReader NGS System
GeneRead Sequencing Q Kits
For preparation of DNA for next-generation sequencing (NGS) applications using ...
    • For high quality sequencing performance
    • Available in kits for multiple flow cell runs
    • Color-coded kit components for easy set-up
    • Proven performance with the GeneReader NGS System
GeneRead QIAcube
ライブラリー・テンプレート調製の自動化および能率化
    • 顕著な手作業時間の短縮と再現性の増大
    • シーケンス用ライブラリー・テンプレート同時調製が1~4 つの間でスケール化可能
    • 直感的なタッチスクリーンでセットアップを通じてガイド
    • 実績のあるQIAcube プラットフォームをベースにした装置
    • GeneReader NGS System で実証済みのバフォーマンス
GeneRead Library Quant System
For qPCR-enabled quantification of NGS libraries
    • Ready-to-use, predispensed, sequentially diluted DNA standard (array format)
    • Automatic calculation of library concentration
    • Simple protocol, high sensitivity, and wide dynamic range
    • Compatibility with Illumina and Ion Torrent/Proton NGS platforms
    • Compatibility with most qPCR instruments
GeneRead Link Software
GeneReader NGS System とLIMS (ラボ情報管理システム)間でのデータ自動転送
    • データをLIMS からGeneReader NGS System へ、そして結果をLIMSに戻すというデータ自動転送
    • 結果をチェックするための労力および時間の削減
    • サンプルに関する全データの履歴管理
    • GeneReader NGS System で実証ずみのパフォーマンス
GeneRead DNA I Amp Kit
For fast and efficient preparation of DNA libraries for use in NGS applications
    • Fast, one-tube procedure that allows up to 50% time savings
    • High yields from minimal amounts of starting material
    • Unbiased amplification with an optional, high-fidelity amplification step
    • Multiplexing, high-throughput capability
GeneRead DNA QuantiMIZE Kits
For quantification and qualification of amplifiable DNA prior to NGS
    • Provides 2 qPCR assays dispensed onto arrays or in individual tubes
    • Quantifies and qualifies DNA that is amplifiable by PCR
    • Guides optimization of targeted enrichment conditions
    • Requires no serial dilutions
GeneRead DNA Library l Core Kit
For fast and efficient preparation of DNA libraries for use in NGS applications
    • Fast, one-tube procedure that allows up to 50% time savings
    • High yields from minimal amounts of starting material
    • Unbiased amplification with an optional, high-fidelity amplification step
    • Multiplexing, high-throughput capability
GeneRead DNA L Amp Kit
For fast and efficient preparation of DNA libraries for use in NGS applications
    • Fast, one-tube procedure that allows up to 50% time savings
    • High yields from minimal amounts of starting material
    • Unbiased amplification with an optional, high-fidelity amplification step
    • Multiplexing, high-throughput capability
GeneRead DNA L Core Kit
For fast and efficient preparation of DNA libraries for use in NGS applications
    • Fast, one-tube procedure that allows up to 50% time savings
    • High yields from minimal amounts of starting material
    • Unbiased amplification with an optional, high-fidelity amplification step
    • Multiplexing, high-throughput capability
QIAsymphony SP for FFPE sample preparation
For automated, high throughput DNA prep from FFPE tissue samples
    • Rapid purification of high-quality, ready-to-use DNA for use in research applications
    • Enzymatic removal of cytosine deamination artifacts for FFPE samples
    • Automation on the QIAsymphony Sample Preparation
    • Outstanding results in DNA sequencing applications
GeneRead QIAact Lung UMI Panels
For all lung cancer insights from FFPE and liquid biopsy* samples
    • All mutation types: SNVs, InDels, CNVs and now fusions
    • Higher sensitivity and more uniform coverage with the unique UMI technology
    • For use with FFPE and liquid biopsy* samples
    • DNA cleanup steps fully automatable on the QIAcube instrument
    • Integrated as part of a complete sample-to-insight NGS workflow including full bioinformatics analysis and interpretation
GeneRead QIAact Custom Panels
For targeted sequencing of the variants most relevant to your research
    • Select the genomic regions of most relevance to your medical research
    • All mutation types: SNVs, InDels, CNVs and fusions
    • For use with FFPE and liquid biopsy samples
    • Uniform sequence coverage enabled by UMI technology
    • Integrated as part of a complete Sample to Insight NGS workflow including full bioinformatics analysis and interpretation
GeneRead Databank
For automated archiving of GeneReader run data
    • Manages data storage for the GeneReader workstation
    • Ensures there is always enough available disc space for the GeneReader to operate
    • Makes stored data searchable and accessible via Microsoft Internet Explorer, Firefox or Google Chrome
    • Allows you to configure your own policies for data storage and clean-up
GeneRead Pure mRNA Kit
For highly selective and efficient purification of mRNA for NGS applications
    • Efficient removal of almost all rRNAs (significantly >99%)
    • No bias from unintended removal of poly A+ mRNAs
    • As little as 100 ng – 5 μg total RNA required
    • Maximal convenience, minimal hands-on time
    • Automation on the QIAcube
GeneRead QIAact BRCA Advanced DNA UMI Panel
For detection of somatic variants from FFPE samples and pathogenic germline variants from ...
    • Complete coverage of the BRCA1, BRCA2, TP53 and most of PTEN
    • Detection, classification & interpretation of somatic and germline variants
    • Detection of SNVs, CNVs (deletions and amplifications) and InDels
    • Incorporating UMI technology for accurate variant detection and quantification
    • A fully integrated assay with the Sample to Insight GeneReader NGS System
GeneRead QIAact AIT DNA UMI Panel
For even more actionable solid tumor insights from FFPE samples
    • Capturing mutations from FFPE samples of solid tumors
    • Covering the most cancer-relevant variants in 30 genes
    • Incorporating unique molecular indices (UMIs) for high analytical sensitivity and specificity for somatic variants
    • For detection of SNV, CNV and small insertion and deletion (<20 bp) variants
    • A complete GeneReader NGS System assay including QCI Analyze and Interpret
EpiTect Hi-C Kit
For high-resolution mapping of chromatin folding, high-quality assembly of genome ...
    • All-inclusive kit – quality-controlled reagents for generating Hi-C NGS libraries
    • Included Illumina adapters with sequence bar codes for multiplex sequencing
    • Fully tested, robust and fast protocol – Hi-C library generation in <2 days
    • Low sample input requirement – libraries generated from just 250,000 cells
    • Data analysis pipeline based on open-source tools
QIAcube Connect

QIAGENサンプルテクノロジーを網羅した新しい自動核酸精製装置

    • 3000以上のプロトコールで80以上のQIAGENキットを自動化
    • DNA、RNA、タンパク質サンプル処理を自動化
    • 手作業による処理手順を排除
    • 標準化された結果を提供
    • 付属のタブレットで迅速に装置の状態をリモート管理
QIAcube

QIAGENスピンカラムキットを用いたサンプル精製の完全自動化

    • 信頼できるQIAGENスピンカラムキットの自動化
    • マニュアル操作ステップを排除
    • DNA、RNA、タンパク質の精製
    • 経済的な自動化サンプル調製で研究時間を確保
    • 標準化された結果と実験操作の効率化
QIAamp Circulating Nucleic Acid Kit

ヒト血漿あるいは血清から遊離DNA/RNAを分離

    • サンプルインプット量を増やし(最高5 ml)、溶出量を減らす(最少20 µl)ことで核酸の高濃縮を実現
    • フラグメント化したDNAおよびRNAを効率的に回収
    • 有機溶媒抽出およびアルコール沈殿不要
    • 夾雑物および阻害物質を除去
QIAact Myeloid DNA UMI Panel

For detection of key mutations in myeloid malignancies from blood and bone marrow

    • Targeting 25 genes of known significance to myeloid malignancies
    • High sensitivity for detection of key variants, enabled by digital sequencing using UMIs
    • Detection of challenging mutations including FLT3 ITDs, CALR deletions and CEBPA mutations
    • Verified as part of our complete Sample to Insight workflow
    • Integrated bioinformatics interpretation and reporting with QCI
QIAGEN Clinical Insight (QCI) Analyze
GeneReader NGS System を構成するバイオインフォマティクパート
    • 最適化され、使いやすく、デザイン済みの2次データ解析パイプライン
    • ラン、編集、レポートの役割ごとやワークフローカスタマイズの管理
    • 迅速で信頼できる世界的に認識されたアルゴリズム
    • レビュープロセスで変異をフィルタリング、確認あるいは拒否できるユニークな性能
    • 完結で明白なレポート
QIAGEN Clinical Insight (QCI) Interpret
NGS データの解釈およびレポーティング用
    • エビデンスに基づいた明白な変異分類
    • 臨床研究の知見を加速させるため薬剤表示および臨床試験に由来する実用的なコンテンツにフォーカス
    • マニュアルで丁寧に精選された臨床関連の所見および生物学的研究にアクセス
    • 簡潔で明確な参照付きレポートをアウトプット
    • 続いて行なう解釈のスピードと正確性を増大するためにユーザーの実験をベースにした個人データベース構築のオプション
GeneReader Platform
次世代シークエンシング(NGS)アプリケーション用
    • 世界初の完結型NGS ワークフロー:サンプル調製から解析までのプロセスを簡便化かつ効率化した完結型シームレス・ワークフロー
    • 実用的なインサイト:QIAGEN の実績ある遺伝子パネルとバイオインフォマティクスに基づく信頼性の高いレポート作成
    • 研究ニーズに柔軟に対応:ニーズに応じて、バッチサイズの拡張および複数のフローセルの連続的なロードが可能
    • 実績ある専門知識やサービスの提供: QIAGEN チームはGeneReader を効率的かつ正しく作動するようにサポートを提供
QIAxpert System
DNA、RNAおよびタンパク質の定量と品質管理を加速
    • 最大16サンプルの核酸を2分以内に測定・定量できる迅速性
    • 革新的な独自のスペクトラルプロトコールで目的の分子を見分けて認識
    • 溶液中のDNA、RNAとその他の夾雑物を各々定量する高い分析能
    • 本体にビルトインされた直感的タッチスクリーンなどの高い操作性
    • 測定結果を他のPCやスマートフォンで閲覧管理できるポータビリティ
QIAseq Targeted DNA Custom Panels

Digital DNA sequencing to confidently detect low-frequency variants

    • Digital sequencing enabled by molecular barcodes to remove PCR duplicates
    • Complete Sample to Insight solution streamlines the workflow
    • Compatibility with low-quality DNA enables efficient sequencing of FFPE and cfDNA samples
    • Minimal DNA input to preserve precious samples
    • Optimized buffers and conditions to achieve high coverage of GC-rich regions
    • Build and receive within two weeks a panel for your unique content
QIAseq DNA QuantiMIZE Kits
For quantification and qualification of amplifiable DNA prior to NGS
    • Provides 2 qPCR assays dispensed onto arrays or in individual tubes
    • Quantifies and qualifies DNA that is amplifiable by PCR
    • Guides optimization of targeted enrichment conditions
    • Requires no serial dilutions
QIAseq Index Kits

For indexing samples enriched with either QIAseq Targeted DNA Panels or QIAseq Targeted ...

      • Sample indexes to index up to 384 samples for Illumina sequencers or 96 samples for Ion Torrent sequencers
      • Enough of each index for four samples
      • Modular indexing structure for Illumina
      • Tube format for flexibility and array format for convenience and high-throughput
    QIAseq Library Quant System
    qPCR によるNGS ライブラリーの定量
      • 即使用可能でプレデザイン済みのアレイフォーマットに分注済みの段階希釈したDNAスタンダード
      • ライブラリー濃度の自動計算
      • 簡単なプロトコール、高い感度、幅広いダイナミックレンジ
      • IlluminaおよびIon Torrent/Proton プラットフォームで使用可能
      • 幅広い種類のqPCR装置で使用可能
    QIAseq cfDNA All-in-One Kits
    For conversion of cfDNA from plasma to NGS library for any liquid biopsy samples
      • Optimal conversion of cfDNA at every step from plasma to NGS library through highly efficient ligation chemistry 
      • Go directly from eluant to library prep without quantification using a protocol supporting the widest range of cfDNA input (1–100ng)  
      • Generate PCR-free libraries from 10 ng of cfDNA
      • Minimize PCR bias by the use of high-fidelity amplification reagents
      • Reduce cross-contamination risk with pre-dispensed plate-based adapters for up to 96 samples/NGS run
    QIAseq FX DNA Library Kit

    High-quality whole genome libraries – no shearing required!

      • DNA fragmentation to NGS-ready libraries – all in a single kit
      • Streamlined 2.5-hour workflow for easy automation
      • High library complexity and even coverage maximizes interpretable data
      • Flexible DNA inputs of 20 pg –1 µg 
      • Customizable fragment and batch sizes match any whole genome or hybrid capture workflow
    QIAseq FX Single Cell DNA Library Kit

    シークエンスフィデリティを持ったシングルセルからの全ゲノムライブラリー調製
      • シングルセルからの全ゲノムライブラリーを4 時間以内に調製
      • ゲノムカバレッジを最大化することで重要な情報を逃さない
      • 偽陽性を低減したシークエンスフィデリティもクラス最高レベル
      • PCR フリーのNGS ライブラリー
      • ゲノム上のどこでも、シークエンス解析とCNV 解析が可能
    QIAseq FX Single Cell RNA Library Kit
    Single cell RNA-seq libraries that provide a deeper view of the transcriptome
      • Higher diversity libraries detect more transcripts, including mRNA and lncRNA
      • PCR-free protocol reduces bias and provides great reproducibility
      • Sequencing ready libraries from isolated single cells in just 5.5 hours
    QIAseq Ultralow Input Library Kit
    イルミナ社の次世代シークエンシング用DNAライブラリー調製
      • サブナノグラムのサンプルにも対応する超効率ケミストリ
      • 10 pg〜100 ngのDNAインプットへの包括的なソリューションを提供する柔軟なプロトコール
      • 96反応キットに含まれるオートメーション対応の二重バーコードアダプタープレート
      • cfDNA、FFPE、古代DNAおよびChIP-seqを含む幅広いサンプルタイプに対応
    QIAsymphony RGQ

    Integrated automated sample preparation and assay setup, with manual transfer to the ...

      • Unprecedented flexibility
      • Workflow optimization and utility
      • Maximized ease of use and convenience
      • Regulated assays and laboratory-developed tests
      • Designed for largest range of applications
    QIAseq Targeted RNA Custom Panels

    For digital RNA-seq for gene expression profiling

      • Use up to 1000 mRNAs or lncRNAs per panel
      • Start with 25 ng of total RNA for each panel
      • Molecular barcodes ensure accurate expression profiling
      • Go from sample to sequence-ready library in 1 day
    QIAseq Targeted RNA Extended Panels
    Digital RNAseq for gene expression profiling
      • Add up to 25 genes to a catalog panel
      • Use only 25 ng of total RNA for each panel
      • Go from sample to sequence-ready library in 1 day
      • Molecular barcodes ensure accurate expression profiling
    QIAseq Targeted RNAscan Panels
    Applying digital RNA sequencing to scan for known and novel fusion genes
      • Accurate quantification of a large number of fusion genes
      • Identify new fusion gene partners, no prior knowledge of breakpoint needed
      • Works with low-quality RNA, including RNA from FFPE and liquid biopsy
      • Requires low RNA input, as low as 15 ng of un-enriched RNA
      • Automation-friendly


    QIAseq Targeted RNA Panels
    Digital RNAseq for gene expression profiling
      • Molecular barcodes remove PCR and library construction bias
      • Start with only 25 ng of total RNA
      • Simple 1 day library construction workflow
      • Use with any illumina or Thermo-Fisher NGS instrument
    QIAseq Targeted RNA Indexes
    For indexing samples for targeted RNA sequencing and primers necessary for sequencing RNA ...
      • Sample indexes to index up to 96 samples for Illumina and Ion Torrent sequencers
      • Enough of each index for four samples
      • Tube format for flexibility and array format for convenience and high-throughput
    QIAseq 1-Step Amplicon DNA Library Kit
    迅速で効率的なNGS用ライブラリー調製
      • PCR産物からワンチューブで30分以内にライブラリー調製
      • 室温での反応セットアップが可能で、一反応で自動化可能
      • イルミナNGSプラットフォームでの使用に適した、高品質でアーティファクトのないライブラリー
      • 1 ngのインプットDNAで、任意の遺伝子パネルまたはPCR産物に適合
      • シングルユースのアダプタープレートにより、コンタミや取り扱いエラーを最小限に
    QIAscout
    お手持ちの倒立顕微鏡で簡単にシングルセルを単離
      • 倒立顕微鏡に組み合わせるだけの簡単セットアップ
      • 様々な真核細胞に対応 細胞
      • 単離後も細胞は生存可能
      • 単離された細胞は様々なシングルセル解析に使用可能
    QIAseq Targeted DNA Extended Panels

    Digital DNA sequencing to confidently detect low-frequency variants

      • Digital sequencing enabled by molecular barcodes to remove PCR duplicates
      • Complete Sample to Insight solution streamlines the workflow
      • Compatibility with low-quality DNA enables efficient sequencing of FFPE and cfDNA samples
      • Minimal DNA input to preserve precious samples
      • Optimized buffers and conditions to achieve high coverage of GC-rich regions
      • Add up to 100 primers to extend the content of a cataloged panel
    QIAseq miRNA Library Kit
    次世代シークエンシングを用いた差次的発現解析と新規遺伝子発見のためのゲルフリー miRNA Sample to Insightソリューション
      • わずか1 ngの全RNAからゲルフリーmiRNAシーケンシングライブラリー調製
      • アダプターダイマーおよび不要RNA種の除去による、最高のフィデリティと高効率データ
      • ビーズベースでのアダプターダイマーおよび不要RNA種除去
      • 個々のmiRNA分子の定量を可能にするIntegrated Unique Molecular Indices(UMI)
      • GeneGlobe Data Analysis Centerを使用した一次リードマッピングおよび差次的発現解析
    QIAseq Targeted DNA Booster Panels

    Digital DNA sequencing to confidently detect low-frequency variants

      • Digital sequencing enabled by molecular barcodes to remove PCR duplicates
      • Complete Sample to Insight solution streamlines the workflow
      • Compatibility with low-quality DNA enables efficient sequencing of FFPE and cfDNA samples
      • Minimal DNA input to preserve precious samples
      • Optimized buffers and conditions to achieve high coverage of GC-rich regions
      • Boost the performance of some primers or extend the content of a custom panel
    QIAseq Targeted RNAscan Custom Panel
    Applying digital RNA sequencing to scan for known and novel fusion genes
      • Accurate quantification of a large number of fusion genes
      • Identify new fusion gene partners, no prior knowledge of breakpoint needed
      • Works with low-quality RNA, including RNA from FFPE and liquid biopsy
      • Requires low RNA input, as low as 15 ng of un-enriched RNA
      • Build and receive within two weeks a panel for your unique content
    QIAseq miRNA Library QC PCR Panel and Assays
    For evaluating RNA sample quality prior to miRNA/small RNA NGS library preparation and ...
      • Unique qPCR-based sample QC of miRNA/small RNA samples prior to NGS
      • Essential for challenging samples with low RNA content, such as biofluids
      • LNA miRNA PCR Assays in ready-to-use PCR panels
      • Compatible with all major qPCR instruments
      • Comprehensive set of 52 RNA spike-ins, spanning a wide range of concentrations
      • Thorough post-sequencing assessment of NGS linearity and reproducibility
    QIAseq Stranded RNA Library Kits
    For preparation of stranded whole transcriptome RNA-seq libraries for NGS applications on ...
        • Stranded, high-quality RNA-seq libraries for transcriptome analysis
        • Only 100–5000 ng of total RNA or 1–100 ng of poly-A+ enriched RNA required
        • No need for actinomycin D and dUTP digestion for stranded library prep
        • Includes QIAseq Beads and dual-barcoded sample adapter plates
        • Compatible with fresh, as well as FFPE samples
    QIAseq Immune Repertoire RNA Library Kits
    For human and mouse immune repertoire screening
      • Unique Molecular Indices (UMI) ensure accurate sequencing results
      • Online data analysis through GeneGlobe
      • Includes QIAseq Beads for reaction cleanup
      • Automation-friendly protocol for human or mouse samples
      • QIAseq Sample Indices ordered separately to multiplex up to 384 samples


    QIAseq UPX 3’ Transcriptome Kits
    For high-throughput 3' transcriptome NGS from ultralow amounts of RNA

      • Start with 1–100 cells or 10 pg to 1 ng of isolated RNA
      • LNA-enhanced chemistry for increased accuracy, specificity and sensitivity
      • UMIs eliminate library amplification bias for accurate gene expression
      • UPX tagging allows 4608–18,432 samples per single sequencing lane    
      • Includes cloud-based read alignment and single-cell or low-input analysis
    QIAseq Targeted DNA Panels

    Digital DNA sequencing to confidently detect low-frequency variants

      • Digital sequencing enabled by molecular barcodes to remove PCR duplicates
      • Complete Sample to Insight solution streamlines the workflow
      • Compatibility with low-quality DNA enables efficient sequencing of FFPE and cfDNA samples
      • Minimal DNA input to preserve precious samples
      • Optimized buffers and conditions to achieve high coverage of GC-rich regions
    QIAseq UPX 3’ Targeted RNA Panels
    For ultraplex (UPX) gene expression analysis using 3' RNA-seq from single cells and ...
      • Target up to 1000 genes using a cost-effective, time-saving single-tube library prep
      • LNA-enhanced chemistry for increased accuracy, specificity and sensitivity
      • UMIs eliminate library amplification bias for accurate gene expression
      • Cell tagging and sample indexing enables simultaneous sequencing of up to 147,456 targeted libraries
      • Includes cloud-based read alignment and single-cell or low-input analysis
    QIAseq Methyl Library Kit
    For robust library preparation for DNA methylation analysis
      • High library yield and mapping rates
      • Low bias and error rates
      • Wide range of DNA input
      • Compatible with cfDNA samples
      • Suitable for enriched fragmented samples (e.g., RRBS, MeDIP)
    QIAseq 16S/ITS Smart Control
    For use with QIAseq 16S/ITS Panels to monitor library construction steps and ...
      • Monitor library construction steps
      • Monitor introduction of potential contamination
    QIAseq 16S/ITS Screening Panel
    For next-generation sequencing-based Sample to Insight profiling of bacterial and fungal ...
      • Interrogate all bacterial 16S rRNA gene variable regions and fungal ITS regions
      • "Phased primers" increase base and read quality
      • Low-bioburden reagents minimize background contamination
      • DNA input as low as 1 pg to profile low-biomass samples
    QIAseq 16S/ITS Region Panels
    For next-generation sequencing-based Sample to Insight profiling of bacterial and fungal ...
      • Interrogate specific bacterial 16S rRNA gene variable regions and fungal ITS regions
      • "Phased primers" increase base and read quality
      • Low-bioburden reagents minimize background contamination
      • DNA input as low as 1 pg to profile low-biomass samples
    QIAseq 16S/ITS Index Kits
    Adapters and sample indexes for constructing libraries using the QIAseq 16S/ITS Panels
      • Sample indexes to index up to 96 samples using Illumina sequencers
      • Sufficient supply of each index for 4 samples
      • Tube format for flexibility and array format for convenience and high throughput
    QIAseq FastSelect RNA Removal Kits
    RNAシークエンシングで重要なrRNAやグロビンmRNAの迅速な除去
      • QIAGEN、Illumina、NEB、KAPA RNA stranded library kitに対応
      • わずか20分でrRNAやグロビンmRNAを高性能除去
      • 必要な手順は 1回のピペッティングのみ – 除去試薬とRNAを混合し、インキュベート
      • クリーンアップステップの追加やプロトコールの修正は不要
      • 動物種とターゲットによりカスタム品の作成も応相談
    QIAseq Tumor Mutational Burden Panels
    For creating a comprehensive profile of Tumor Mutational Burden (TMB) and Microsatellite ...
      • Create highly uniform libraries
      • Easy workflow using enzymatic fragmentation
      • Robust analysis modules
      • Unprecedented insight
    QIAseq FastSelect –rRNA HMR Kits
    For rapid rRNA and/or globin mRNA removal for RNA-seq library preparation from ...
      • Compatible with QIAGEN, Illumina, NEB and KAPA stranded RNA-seq library kits
      • Single reagent for human, mouse, rat and other mammalian species
      • High-performance rRNA and/or globin removal in just 14 minutes
      • Only one pipetting step – combine QIAseq FastSelect reagent with RNA and incubate
      • No extra cleanup steps or NGS library protocol changes
    QIAseq FastSelect –5S/16S/23S Kits
    For rapid 5S/16S/23S rRNA removal for RNA-seq library preparation from bacterial RNA ...
      • Pan-bacterial 5S/16S/23S rRNA removal from fragmented or full-length RNA for metatranscriptomics studies
      • Novel RNA removal mechanism that doesn't involve hybrid capture or enzymatic digestion
      • Combine with QIAseq FastSelect –rRNA HMR for removal of human, mouse, rat rRNA for host-microbe studies
      • Verified performance with QIAGEN, Illumina and NEB RNA-seq library kits without workflow changes
      • In-silico design predicts blocking of >95% of all 5S, 16S and 23S rRNA database sequences