Showing 81 - 100 results of 1,757 for search '"The Indelicates"', query time: 0.10s Refine Results
  1. 81

    MYCOBACTERIUM TUBERCULOSIS GENOME INDEL AND CRISPRI HIGH- THROUGHPUT SCREENING BY MANIPULATING ITS ENDOGENOUS TYPE IIIA CRIPSR by M.A. Naeem, K. Rahman, W. Ahmad, Z. Habib

    Published 2023-05-01
    “…Guide RNA for the target gene was designed and homology- directed repair (HDR) sequence containing GFP was employed for gene insertion- deletion (indel). For gene knock-down (RNA interference) mechanism was identified by RIP-qPCR. …”
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    Article
  2. 82

    Tool evaluation for the detection of variably sized indels from next generation whole genome and targeted sequencing data. by Ning Wang, Vladislav Lysenkov, Katri Orte, Veli Kairisto, Juhani Aakko, Sofia Khan, Laura L Elo

    Published 2022-02-01
    “…Insertions and deletions (indels) in human genomes are associated with a wide range of phenotypes, including various clinical disorders. …”
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    Investigating structural variant, indel and single nucleotide polymorphism differentiation between locally adapted Atlantic salmon populations by Laurie Lecomte, Mariann Árnyasi, Anne‐Laure Ferchaud, Matthew Kent, Sigbjørn Lien, Kristina Stenløkk, Florent Sylvestre, Louis Bernatchez, Claire Mérot

    Published 2024-03-01
    “…We first catalogued polymorphism using a hybrid SV characterization approach pairing both short‐ (16X) and long‐read sequencing (20X) for variant discovery with graph‐based genotyping of SVs across 60 salmon genomes, along with characterization of SNPs and small indels from short reads. We thus identified 115,907 SVs, 8,777,832 SNPs and 1,089,321 short indels, with SVs covering 4.8 times more base pairs than SNPs. …”
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  5. 85

    Association between an indel polymorphism within the distal promoter of EGLN2 and cancer risk: An updated meta‐analysis by Shulong Zhang, Kaihua Zhu, Zuoliang Zhang, Hui Wang, Xiaolong Wang

    Published 2019-10-01
    “…Abstract Background The association between a 4‐bp indel polymorphism (rs10680577) within the distal promoter of EGLN2 and cancer risk has been investigated by several case–control studies in recent years, but investigation results were inconsistent. …”
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  6. 86

    High-Throughput Sequencing of Phage Display Libraries Reveals Parasitic Enrichment of Indel Mutants Caused by Amplification Bias by Sander Plessers, Vincent Van Deuren, Rob Lavigne, Johan Robben

    Published 2021-05-01
    “…This revealed enriched genotypes with small indels and concomitant doubtful amino acid motifs within the FTO library. …”
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  7. 87

    MetaRNN: differentiating rare pathogenic and rare benign missense SNVs and InDels using deep learning by Chang Li, Degui Zhi, Kai Wang, Xiaoming Liu

    Published 2022-10-01
    “…Using context annotations and deep learning methods, we present pathogenicity prediction models, MetaRNN and MetaRNN-indel, to help identify and prioritize rare nonsynonymous single nucleotide variants (nsSNVs) and non-frameshift insertion/deletions (nfINDELs). …”
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    Prevalence of BRCA homopolymeric indels in an ION Torrent-based tumour-to-germline testing workflow in high-grade ovarian carcinoma by Jacopo Azzollini, Luca Agnelli, Elena Conca, Tommaso Torelli, Adele Busico, Iolanda Capone, Marta Angelini, Elena Tamborini, Federica Perrone, Andrea Vingiani, Daniele Lorenzini, Bernard Peissel, Giancarlo Pruneri, Siranoush Manoukian

    Published 2023-05-01
    “…The low sensitivity for indels at loci with sequences of identical bases (homopolymers) of ion semiconductor-based sequencing techniques represents a well-known limitation, but the prevalence of indels overlooked by these techniques in high-risk populations has not been investigated. …”
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    Genome-Wide Discovery of InDel Markers in Sesame (<i>Sesamum indicum</i> L.) Using ddRADSeq by Sibel Kizil, Merve Basak, Birgul Guden, Hilal Sule Tosun, Bulent Uzun, Engin Yol

    Published 2020-09-01
    “…On average, InDels of at least 2 bp in length had a frequency of 2.99 InDels/Mb. …”
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  15. 95

    An Indel Polymorphism in the MtnA 3' Untranslated Region Is Associated with Gene Expression Variation and Local Adaptation in Drosophila melanogaster. by Ana Catalán, Amanda Glaser-Schmitt, Eliza Argyridou, Pablo Duchen, John Parsch

    Published 2016-04-01
    “…Insertions and deletions (indels) are a major source of genetic variation within species and may result in functional changes to coding or regulatory sequences. …”
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    Article
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