Labshake search
Citations for Illumina :
7001 - 7050 of 10000+ citations since 2019
Citations are collected from bioRxiv only, the total number of publications could be much larger.
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bioRxiv - Genomics 2023Quote: Nuclei were treated with 2.5 µl of Tn5 Transposase (Illumina) in the standard tagmentation reaction buffer (25 µl) ...
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bioRxiv - Genomics 2023Quote: Final libraries were sequenced on the NextSeq2000 (Illumina, San Diego, CA, USA) as recommended by 10X Genomics (Read 1 ...
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bioRxiv - Evolutionary Biology 2023Quote: ... Additional sequencing was performed on a NovaSeq 6000 sequencer (Illumina, San Diego ...
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bioRxiv - Evolutionary Biology 2023Quote: ... libraries were produced from 50 ng of DNA with the Nextera XT DNA Sample Preparation Kit (Illumina, Germany) according to the manufacturer’s protocol ...
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bioRxiv - Genomics 2023Quote: ... and patient-derived LCLs was used for SNP-array copy number profiling and analysis of regions of homozygosity with the Infinium Human CytoSNP-850K v1.2 BeadChip (Illumina, San Diego, CA, USA). This array has ∼850,000 single nucleotide polymorphisms (SNPs ...
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bioRxiv - Genetics 2023Quote: ... Strand-specific sequencing libraries were generated using TruSeq stranded total RNA library preparation kit (Illumina Inc. Cat # 20020596) and sequenced as 75bp paired-end reads on an Illumina instrument.
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bioRxiv - Genomics 2023Quote: ... WGS libraries were generated using standard protocols (Illumina). Libraries were sequenced to 15-30x genome coverage (2×150bp ...
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bioRxiv - Evolutionary Biology 2023Quote: ... and constructed libraries using Illumina TruSeq DNA PCR-Free (Illumina, San Diego, CA, USA) or Illumina DNA Prep ...
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bioRxiv - Genomics 2023Quote: ... Samples were then loaded onto the Illumina NextSeq500 Instrument using a Mid-output 300 cycle kit (Illumina Catalogue FC-404-2003) or the MinION flow cell ONT instrument (R9.4.1) ...
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bioRxiv - Genomics 2023Quote: ... and used 1 ng for DNA library preparation using the Nextera XT DNA Library Preparation kit (Illumina), according to manufacturer’s protocol ...
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bioRxiv - Genomics 2023Quote: ... The Nextera HT kit (Illumina) was used to convert cDNA libraries into sequencing libraries with the addition of a UMI-specific primer to amplify the cDNA ends containing molecular barcodes as described in the Smart-seq3 protocol ...
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bioRxiv - Genomics 2023Quote: Preparation of libraries for SMS for both Illumina (Illumina DNA Prep Kit: 20018704) and ONT (Illumina® DNA Prep ...
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bioRxiv - Genomics 2023Quote: ... and ONT (Illumina® DNA Prep ...
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bioRxiv - Genomics 2023Quote: Pelleted nuclei were gently resuspended in a 50 μL transposition reaction mix composed of 25 μL 2× TD Buffer (Illumina), 2.5 μL Tn5 Transposes (Illumina ...
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bioRxiv - Genomics 2023Quote: ... Nextera Library Preparation Biochemistry (Illumina) was used to prepare sequencing libraries ...
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bioRxiv - Genomics 2023Quote: ... 2.5 μL Tn5 Transposes (Illumina) and 22.5 μL Nuclease-Free H2O ...
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bioRxiv - Genomics 2023Quote: ... Each individual received a unique barcode before multiplexing individuals (Illumina NovaSeq 6000; 2×150bp PE lane).
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bioRxiv - Genomics 2023Quote: ... The prepared library was sequenced on Illumina NovaSeq 6000 instrument (Illumina Inc., USA) for paired-end sequencing ...
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bioRxiv - Genomics 2023Quote: ... and sequenced by Illumina HiSeq 4000 (Illumina, San Diego, USA). After filtering out low quality and duplicated reads ...
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bioRxiv - Genomics 2023Quote: ... chrRNA were then subjected to library preparation using True-seq stranded total RNA library prep gold kit (Ref#220599) from Illumina using 1 μg of chrRNA ...
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bioRxiv - Genomics 2023Quote: ... and sequenced on Illumina HiSeq X instrument (Illumina Inc., USA) for 150 bp paired-end reads ...
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bioRxiv - Genomics 2023Quote: ... and sequenced by PacBio Sequel II. Hi-C libraries were prepared following a standard protocol (Belton et al. 2012) and sequenced by Illumina HiSeq 4000 (Illumina ...
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bioRxiv - Genomics 2023Quote: ... Samples were diluted to 200 pg/μL or 100 pg/μL for Nextera XT (Illumina) library preparation in respectively one-fourth or one-tenth of the volume recommended by the manufacturer using manual or automated liquid handling ...
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bioRxiv - Genomics 2023Quote: ... Five ng of ChIP DNA were used to prepare sequencing libraries with Illumina ChIP Sample Library Prep Kit (Illumina, USA). After end-repair and adaptor ligation ...
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bioRxiv - Genomics 2023Quote: Prepared libraries were sequenced on a NovaSeq 6000 (Illumina, Sand Diego CA, USA) to a mean on-target duplex depth of ∼16,000x ...
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bioRxiv - Genomics 2023Quote: ... All libraries were loaded at 1.8pM onto a NextSeq500 (Illumina) and sequenced using a high output reagent kit (Illumina ...
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bioRxiv - Genomics 2023Quote: ... Libraries were prepared according to the Nextera XT (Illumina) library preparation protocol and then sequenced using the Illumina MiSeq platform.
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bioRxiv - Genomics 2023Quote: ... using indels called in any of the germline sequencing data of the individual (i.e., both GATK and DeepVariant indel calls when using Illumina germline sequencing data ...
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bioRxiv - Genomics 2023Quote: ... and Hi-C (Illumina NovaSeq 6000, 2×150bp) for chromosome-level scaffolding (Fig ...
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bioRxiv - Genomics 2023Quote: Illumina germline and tumor sequencing libraries were prepared using the TruSeq DNA PCR-Free kit (Illumina) for all samples ...
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bioRxiv - Genomics 2023Quote: ... Sequencing was done using a HiSeq 2500 (Illumina).
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bioRxiv - Genomics 2023Quote: Illumina sequencing reads (∼54 million paired end reads per sample) were de-multiplexed generating compressed FASTQ files by the on-board DRAGEN informatics pipeline (Illumina DRAGEN FASTQ Generation – 3.7.4) on the NextSeq 2000 ...
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bioRxiv - Genomics 2023Quote: ... except GM10430 that used the TruSeq DNA Nano kit (Illumina). At least 110 Gb (∼36x genome coverage ...
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bioRxiv - Genomics 2023Quote: Illumina sequencing reads (∼50 million paired end reads per sample) were de-multiplexed generating compressed FASTQ files by the on-board DRAGEN informatics pipeline (Illumina DRAGEN FASTQ Generation – 3.7.4) on the NextSeq 2000 ...
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bioRxiv - Genomics 2023Quote: ... The library was sequenced on NovaSeq 6000 (Illumina, 2×151bp) following the manufacturer’s protocol for dual indexing.
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bioRxiv - Genomics 2023Quote: ... These five tissue-specific samples were subjected to Illumina’s TruSeq Stranded mRNA library preparation kit and sequenced on NovaSeq 6000 (Illumina, 2×150 bp). For long-read RNA sequencing ...
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bioRxiv - Genomics 2023Quote: ... The library was sequenced on NovaSeq 6000 (Illumina, 2×151bp) following the manufacturer’s protocol for dual indexing ...
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bioRxiv - Genomics 2023Quote: ... We generated libraries from three independent biological replicates and sequenced them separately with a NovaSeq 6000 (Illumina). FASTQ files generated from each sequencing run were pooled and analyzed using the cellranger-atac aggr v2.0 pipeline ...
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bioRxiv - Genomics 2023Quote: ... At least 110 Gb (∼36x genome coverage) of 150-base pair paired-end sequencing per sample was obtained using a Novaseq 6000 instrument (Illumina) by Psomagen Inc ...
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bioRxiv - Genomics 2023Quote: ... Illumina sequencing reads (∼6 million paired end reads per sample) were de-multiplexed generating compressed FASTQ files by the on-board DRAGEN informatics pipeline (Illumina DRAGEN FASTQ Generation – 3.7.4) on the NextSeq 2000 ...
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bioRxiv - Genomics 2023Quote: ... The cDNAs from each cell were pooled and a library was generated and sequenced with a NovaSeq 6000 (Illumina). We sequenced two biological replicates to a sequencing depth of ∼1 billion reads each ...
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bioRxiv - Genomics 2023Quote: ... The liver libraries were pooled and paired-end sequenced on the NextSeq 2000 platform (Illumina) using the P2 or P3 100 cycle kit ...
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bioRxiv - Genomics 2023Quote: ... The RNA-seq libraries were subjected to two rounds of 75bp paired end sequencing on a NextSeq 550 platform using a 150-cycle kit (Illumina).
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bioRxiv - Genomics 2023Quote: ... and sequenced on NextSeq 500 (Illumina, paired-end) at the NIEHS Epigenomics Core Facility ...
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bioRxiv - Genomics 2023Quote: The Nextera XT Index Kit (Illumina Inc.) was used for the first amplicon generation followed by NGS library preparation of the QC passed samples ...
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bioRxiv - Genomics 2023Quote: ... The QC passed libraries were sequenced on the MiSeq platform (Illumina) using 2 x 300bp chemistry to generate ~1 lakh reads per sample.
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bioRxiv - Evolutionary Biology 2023Quote: ... 28 and 272-base reads on a NextSeq 2000 sequencer (Illumina). Phylogenies were reconstructed using Cassiopeia [Jones et al. ...
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bioRxiv - Evolutionary Biology 2023Quote: We used both short read transcriptomes generated by Illumina sequencing and long read transcriptomes generated by Iso-seq to construct a high coverage transcriptome ...
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bioRxiv - Genomics 2023Quote: ... and sequenced using a high output reagent kit (Illumina) at the Institute for Molecular Bioscience Sequencing Facility ...
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bioRxiv - Genomics 2023Quote: ... The RNA sequencing was performed on a NovaSeq6000 (Illumina) at IMGM Laboratories GmbH (Martinsried ...