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kapa library preparation hyper plus kit  (Roche)


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    Structured Review

    Roche kapa library preparation hyper plus kit
    Kapa Library Preparation Hyper Plus Kit, supplied by Roche, used in various techniques. Bioz Stars score: 99/100, based on 5 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/kapa+library+preparation+hyper+plus+kit/HyperPrep/pm37997798-41-12-18
    Average 99 stars, based on 5 article reviews
    kapa library preparation hyper plus kit - by Bioz Stars, 2026-09
    99/100 stars

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    Related Articles

    Next-Generation Sequencing:

    Article Title: Comparative Analysis of miRNA and EMT Markers in Metastatic Colorectal Cancer.
    Article Snippet: .. Indexed Illumina NGS library was constructed from 100 ng tumor DNA by KAPA Library Preparation Hyper Plus Kit (Kapa Biosystems). .. Hybrid selection was performed with a custom SeqCap EZ Choice Library (Roche NimbleGen).

    Article Title: Role of N-Cadherin in Epithelial-to-Mesenchymal Transition and Chemosensitivity of Colon Carcinoma Cells.
    Article Snippet: .. Indexed Illumina NGS library was constructed from 100 ng tumor DNA by KAPA Library Preparation Hyper Plus Kit (Kapa Biosystems). .. Hybrid selection was performed with a custom SeqCap EZ Choice Library (Roche NimbleGen).

    Construct:

    Article Title: Comparative Analysis of miRNA and EMT Markers in Metastatic Colorectal Cancer.
    Article Snippet: .. Indexed Illumina NGS library was constructed from 100 ng tumor DNA by KAPA Library Preparation Hyper Plus Kit (Kapa Biosystems). .. Hybrid selection was performed with a custom SeqCap EZ Choice Library (Roche NimbleGen).

    Article Title: Role of N-Cadherin in Epithelial-to-Mesenchymal Transition and Chemosensitivity of Colon Carcinoma Cells.
    Article Snippet: .. Indexed Illumina NGS library was constructed from 100 ng tumor DNA by KAPA Library Preparation Hyper Plus Kit (Kapa Biosystems). .. Hybrid selection was performed with a custom SeqCap EZ Choice Library (Roche NimbleGen).

    Article Title: HPV Status and Mutation Analysis Using Multiparallel Sequencing in Distal Oesophageal and Gastro-oesophageal Junction Adenocarcinomas.
    Article Snippet: HPV DNa detection was performed by real-time Pcr with the amoyDx Human Papillomavirus genotyping Detection kit (amoy Diagnostic co., Fuijan, china) according to the manufacturer’s protocol. the test is designed for detection and genotyping of 19 highrisk HPVs (HPV16, 18, 26, 31, 33, 35, 39, 45, 51, 52, 53, 56, 58, 59, 66, 68, 70, 73, and 82) and two low-risk HPVs (HPV6 and 11). .. Mutation analysis was performed by multiparallel sequencing. indexed illumina NgS library was constructed from 100 ng tumour DNa by a kaPa library Preparation Hyper Plus kit (kapa Biosystems, roche). .. Hybrid selection was performed with a custom Seqcap eZ choice library (roche Nimblegen). the library was designed using genome build hg19 NcBi Build 37.1/grch37. genes in the sequencing panel included (transcript reference numbers are in brackets) ARID1A (NM_006015), BRCA1 (NM_007294), BRCA2 (NM_000059), CDKN2A (NM_000077), CTNNB1 (NM_001904), EGFR (NM_005228), EPHB2-ERK (NM_004442), ERBB2 (NM_004448), ESR1 (NM_000125), FBXW7 (NM_033632), FOXL2 (NM_023067), GNA11 (NM_002067), GNAQ (NM_002072), HRAS (NM_176795), KIT (NM_000222), KRAS (NM_004985), MDM2 (NM_002392), MET (NM_001127500), MLH1 (NM_000249), MSH2 (NM_000251), MSH6 (NM_000179), NotcH1 (NM_017617), NraS (NM_002524), PDGFRA (NM_006206), PIK3CA (NM_006218), PMS2 (NM_000535), PTEN (NM_000314), SMARCA4 (NM_001128844), SMARCB1 (NM_003073), TP53 (NM_000546), ALK (NM_004304), APC (NM_000038), FGFR2 (NM_000141), MAP2K1 (NM_002755), CDH1 (NM_004360), SMAD4 (NM_005359), STK11 (NM_000455), SRC (NM_005417), GNAS (NM_000516), IDH1 (NM_005896), and IDH2 (NM_002168).

    Mutagenesis:

    Article Title: HPV Status and Mutation Analysis Using Multiparallel Sequencing in Distal Oesophageal and Gastro-oesophageal Junction Adenocarcinomas.
    Article Snippet: HPV DNa detection was performed by real-time Pcr with the amoyDx Human Papillomavirus genotyping Detection kit (amoy Diagnostic co., Fuijan, china) according to the manufacturer’s protocol. the test is designed for detection and genotyping of 19 highrisk HPVs (HPV16, 18, 26, 31, 33, 35, 39, 45, 51, 52, 53, 56, 58, 59, 66, 68, 70, 73, and 82) and two low-risk HPVs (HPV6 and 11). .. Mutation analysis was performed by multiparallel sequencing. indexed illumina NgS library was constructed from 100 ng tumour DNa by a kaPa library Preparation Hyper Plus kit (kapa Biosystems, roche). .. Hybrid selection was performed with a custom Seqcap eZ choice library (roche Nimblegen). the library was designed using genome build hg19 NcBi Build 37.1/grch37. genes in the sequencing panel included (transcript reference numbers are in brackets) ARID1A (NM_006015), BRCA1 (NM_007294), BRCA2 (NM_000059), CDKN2A (NM_000077), CTNNB1 (NM_001904), EGFR (NM_005228), EPHB2-ERK (NM_004442), ERBB2 (NM_004448), ESR1 (NM_000125), FBXW7 (NM_033632), FOXL2 (NM_023067), GNA11 (NM_002067), GNAQ (NM_002072), HRAS (NM_176795), KIT (NM_000222), KRAS (NM_004985), MDM2 (NM_002392), MET (NM_001127500), MLH1 (NM_000249), MSH2 (NM_000251), MSH6 (NM_000179), NotcH1 (NM_017617), NraS (NM_002524), PDGFRA (NM_006206), PIK3CA (NM_006218), PMS2 (NM_000535), PTEN (NM_000314), SMARCA4 (NM_001128844), SMARCB1 (NM_003073), TP53 (NM_000546), ALK (NM_004304), APC (NM_000038), FGFR2 (NM_000141), MAP2K1 (NM_002755), CDH1 (NM_004360), SMAD4 (NM_005359), STK11 (NM_000455), SRC (NM_005417), GNAS (NM_000516), IDH1 (NM_005896), and IDH2 (NM_002168).

    Sequencing:

    Article Title: HPV Status and Mutation Analysis Using Multiparallel Sequencing in Distal Oesophageal and Gastro-oesophageal Junction Adenocarcinomas.
    Article Snippet: HPV DNa detection was performed by real-time Pcr with the amoyDx Human Papillomavirus genotyping Detection kit (amoy Diagnostic co., Fuijan, china) according to the manufacturer’s protocol. the test is designed for detection and genotyping of 19 highrisk HPVs (HPV16, 18, 26, 31, 33, 35, 39, 45, 51, 52, 53, 56, 58, 59, 66, 68, 70, 73, and 82) and two low-risk HPVs (HPV6 and 11). .. Mutation analysis was performed by multiparallel sequencing. indexed illumina NgS library was constructed from 100 ng tumour DNa by a kaPa library Preparation Hyper Plus kit (kapa Biosystems, roche). .. Hybrid selection was performed with a custom Seqcap eZ choice library (roche Nimblegen). the library was designed using genome build hg19 NcBi Build 37.1/grch37. genes in the sequencing panel included (transcript reference numbers are in brackets) ARID1A (NM_006015), BRCA1 (NM_007294), BRCA2 (NM_000059), CDKN2A (NM_000077), CTNNB1 (NM_001904), EGFR (NM_005228), EPHB2-ERK (NM_004442), ERBB2 (NM_004448), ESR1 (NM_000125), FBXW7 (NM_033632), FOXL2 (NM_023067), GNA11 (NM_002067), GNAQ (NM_002072), HRAS (NM_176795), KIT (NM_000222), KRAS (NM_004985), MDM2 (NM_002392), MET (NM_001127500), MLH1 (NM_000249), MSH2 (NM_000251), MSH6 (NM_000179), NotcH1 (NM_017617), NraS (NM_002524), PDGFRA (NM_006206), PIK3CA (NM_006218), PMS2 (NM_000535), PTEN (NM_000314), SMARCA4 (NM_001128844), SMARCB1 (NM_003073), TP53 (NM_000546), ALK (NM_004304), APC (NM_000038), FGFR2 (NM_000141), MAP2K1 (NM_002755), CDH1 (NM_004360), SMAD4 (NM_005359), STK11 (NM_000455), SRC (NM_005417), GNAS (NM_000516), IDH1 (NM_005896), and IDH2 (NM_002168).



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