Labshake search
Citations for Illumina :
2951 - 3000 of 10000+ citations for Creatinine Serum Low Sample Volume Kit 384 well Plate since 2019
Citations are collected from bioRxiv only, the total number of publications could be much larger.
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bioRxiv - Plant Biology 2020Quote: ... Libraries were constructed using TruSeq Stranded mRNA Sample PrepKit (Illumina, San Diego, CA, USA) following manufacturer’s instructions ...
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bioRxiv - Evolutionary Biology 2019Quote: ... Samples were sequenced using single-end 75 bp chemistry on the NextSeq 500 (Illumina). Three additional sea anemone datasets (Diadumene lineata ...
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bioRxiv - Cell Biology 2021Quote: ... The library for each sample was sequenced by illumina sequencer (Illumina, San Diego, CA) on a 150 bp paired-end run.
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bioRxiv - Neuroscience 2020Quote: ... All samples proceeded through Nextera XT DNA Library Preparation (Illumina Cat# FC-131-1096) using Nextera XT Index Kit V2 (Illumina Cat# FC-131-2001 ...
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bioRxiv - Genomics 2020Quote: ... The resulting libraries were sequenced with one sample per lane using the NextSeq500 (Illumina; high-output mode ...
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bioRxiv - Evolutionary Biology 2021Quote: ... Samples were paired-end sequenced (2×300 bp) on a MiSeq platform (Illumina, USA) using the MiSeq Reagent kit v3 (Illumina ...
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bioRxiv - Microbiology 2021Quote: ... The normalized samples were sequenced on the Illumina MiSeq platform (Illumina, San Diego, CA) using 300+300 bp paired-end V3 chemistry ...
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bioRxiv - Microbiology 2019Quote: ... Bacteria were grown at 30° g of total RNA in each sample (Illumina Company). Libraries were quantified using a combination of Qubit and Bioanalyzer (Agilent Technologies ...
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bioRxiv - Immunology 2020Quote: ... Indexed samples were sequenced at 100bp-paired-end protocol with the NovaSeq 6000 (Illumina), generating approximately 20-30 million reads per sample ...
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bioRxiv - Immunology 2020Quote: ... All samples were sequenced using an Illumina NovaSeq 6000 sequencer (Illumina, San Diego,CA) with an average of 23 million paired-end reads (2x 50 bp ...
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bioRxiv - Immunology 2021Quote: ... Multiplexing of the samples was achieved using IDT–TruSeq RNA UD Indexes (Illumina, USA). The libraries were then loaded on a S1 Flowcell using the Xp Workflow and subjected to 100 cycles paired-end sequencing on the Illumina NovaSeq 6000 System.
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bioRxiv - Genomics 2021Quote: ... libraries were generated using a modified Illumina Nextera Sample Prep (Illumina, FC-121-1030) protocol ...
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bioRxiv - Genetics 2019Quote: Samples were genotyped using the Global Screening Array v.1.0 from Illumina (636,139 markers). Sample-based (missingness ...
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bioRxiv - Genomics 2021Quote: ... 50 million 50 bp paired-end reads per sample using the HiSeq 4000 (Illumina) device
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bioRxiv - Genomics 2021Quote: For each sample sequenced in 3 separate experiments (CoronaHiT-ONT, CoronaHiT-Illumina, ARTIC-ONT), a phylogeny was generated from all of the consensus genomes (n=216 for the routine samples and n=132 for the rapid response samples ...
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bioRxiv - Genomics 2020Quote: ... Samples were indexed and sequenced on the S4 flow cell of NovaSeq 6000 (Illumina).
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bioRxiv - Genomics 2020Quote: ... Up to four sample libraries were sequenced on the HiSeq X Version 2.5 (Illumina) with the following paired end read configuration ...
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bioRxiv - Genomics 2020Quote: ... the viral pool sample (ViralPool) with Nextera Flex for Enrichment (Illumina, Catalog no. 20025524) and IDT for Illumina Nextera DNA UD Indexes (Illumina ...
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bioRxiv - Genomics 2021Quote: Sample genotyping was performed using the Infinium Illumina Global Screening Array v3.0 (Illumina, 20030770) by the Broad Institute Genomic Services group ...
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bioRxiv - Evolutionary Biology 2021Quote: ... sample 2 was treated with 20 U RNase R (Epicentre/Illumina, Cat. No. RNR07250) for 1 h at 37°C to degrade linear RNAs ...
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bioRxiv - Cancer Biology 2022Quote: ... samples were sequenced using NextSeq500 high output 75nt PE flow cell instrument (ATGC Illumina Next Generation Sequencing Core facility ...
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bioRxiv - Cancer Biology 2022Quote: ... The indexed samples were sequenced on the MiSeq sequencer (Illumina, Inc. San Diego, CA) with 150-base paired-end reads in order to generate >1400X average target coverage after PCR duplicate removal with the use of unique molecular indexes (UMIs) ...
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bioRxiv - Bioengineering 2022Quote: ... 227 samples were sequenced in paired-end modus (PE275) using a MiSeq system (Illumina) according to the manufacturer’s instructions.
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Discovery of malathion resistance QTL in Drosophila melanogaster using a bulked phenotyping approachbioRxiv - Genetics 2022Quote: ... we used 400-ng of each DNA sample to construct indexed sequencing libraries (Illumina DNA Prep Tagmentation ...
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bioRxiv - Genomics 2022Quote: ... Samples were multiplexed into a single library and sequenced on an Illumina HiSeq2500 (Illumina). This library was sequenced across three lanes to achieve the desired number of reads.
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bioRxiv - Microbiology 2022Quote: ... with mean sequencing depth of 130,000 reads per sample (Illumina, Inc. San Diego, CA). The EMP 16S Read 1 ...
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bioRxiv - Neuroscience 2022Quote: ... Libraries from different samples were pooled and sequenced on a NextSeq 500 instrument (Illumina).
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bioRxiv - Immunology 2022Quote: ... normalized libraries were pooled across samples and sequenced on a MiniSeq or NextSeq500 (Illumina). Barcode distribution was analyzed and log2 fold change of barcode representation in output vs input population was calculated to detect changes in abundance ...
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bioRxiv - Cancer Biology 2022Quote: ... Samples were run using 50-cycle paired-end reads on the NovaSeq 6000 (Illumina) to a depth of 100,000 reads ...
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bioRxiv - Molecular Biology 2024Quote: ... Libraries were sequenced to 50 million reads per sample on a NovaSeq 6000 (Illumina) paired end 100 bp and reads processed using bcl2fastq version ...
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bioRxiv - Microbiology 2023Quote: ... Each library consisting of four pooled samples was sequenced on the NextSeq 500 (Illumina) using a 75 base pair cycle sequencing kit (Illumina ...
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bioRxiv - Neuroscience 2024Quote: ... Samples were multiplexed and sequencing were performed using NovaSeq S1 100nt Flowcell v1.5 (Illumina).
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bioRxiv - Cancer Biology 2023Quote: ... Samples were sequenced single-end (1 × 50 bp) on the HiSeq 2500 platform (Illumina) or paired-end (2 × 100 bp ...
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bioRxiv - Developmental Biology 2024Quote: ... Samples were sequenced with 36 bp pair-end reads on the NextSeq 550 (Illumina) using the Illumina NextSeq 500/550 High Output Kit v2.5 (75 cycles ...
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bioRxiv - Cancer Biology 2022Quote: ... All ten samples were sequenced in four runs by a NovaSeq 6000 sequencer (Illumina) to generate paired-end 100bp reads ...
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bioRxiv - Genomics 2023Quote: ... All samples were then processed using the EPIC 850K array (Illumina Inc, CA, USA) according to the manufacturer’s instructions ...
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bioRxiv - Genetics 2023Quote: ... (2014)[32] used 825 samples and the gene expression data were generated from Illumina Human HT-12 V3 BeadChips ...
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bioRxiv - Genetics 2023Quote: ... all RNA samples were diluted to 93.3 ng/uL in ELB buffer (Illumina #20020599). Next ...
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bioRxiv - Developmental Biology 2023Quote: ... and the TruSeq stranded mRNA Library prep (Illumina, San Diego, CA, USA; E12.5 samples) and sequenced with the Illumina Hiseq4000 platform (2×75 PE).
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bioRxiv - Genomics 2022Quote: ... The samples were genotyped using the Illumina BovineHD Beadchip (Illumina Inc., San Diego, CA) genotyping array (777K) ...
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Accumulation of TCR signaling from self-antigens in naive CD8 T cells mitigates early responsivenessbioRxiv - Immunology 2023Quote: ... Samples were sequenced at the Emory Nonhuman Primate Genomics Core on a NovaSeq6000 (Illumina) using PE100 ...
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bioRxiv - Microbiology 2023Quote: ... The libraries were prepared according to the TruSeq Stranded mRNA Sample Preparation Guide (Illumina). Briefly ...
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bioRxiv - Cancer Biology 2023Quote: ... RNA-seq library was constructed following the TruSeq RNA Sample Preparation v2 Guide (Illumina). Briefly ...
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bioRxiv - Microbiology 2023Quote: ... Only those samples that passed the quality check were selected for high-throughput (Illumina) sequencing.
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bioRxiv - Molecular Biology 2023Quote: ... Samples were processed for using NextSeq 1000/2000 P2 Reagents (Illumina, San Diego, CA). Samples were sequenced on the Illumina Hi Seq 2000 platform in the UCL Genomics Facility ...
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bioRxiv - Cancer Biology 2023Quote: ... The samples were then submitted to the for Miseq and Novaseq deep sequencing (Illumina). Two technical replicates were performed on cells from the same library transformation ...
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bioRxiv - Immunology 2023Quote: ... Samples were clustered onto a flowcell and sequenced on the Illumina hiSeq 4000 (Illumina) with 2×150 bp paired end reads ...
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bioRxiv - Molecular Biology 2023Quote: ... Raw sequence reads were demultiplexed into sample-specific fastq files (bcl2fastq program v2.20.0.422, Illumina). The resulting fastq files were processed as follows ...
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bioRxiv - Neuroscience 2024Quote: ... DNA samples were prepared as libraries for sequencing using the Nextera DNA Flex (Illumina) kit and sequenced on an Illumina NextSeq500.
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bioRxiv - Genetics 2024Quote: ... Sample specific genotypes for using with WASP were generated using Omni 2.5M arrays (Illumina) and imputed using the Michigan Imputation Server92,93 (https://imputation.biodatacatalyst.nhlbi.nih.gov/) ...