Labshake search
Citations for Illumina :
2451 - 2500 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 - Developmental Biology 2022Quote: ... Each well was mixed with 0.8 μl Nextera tagmentation DNA buffer (Illumina) and 0.4 μl Tn5 enzyme (Illumina) ...
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bioRxiv - Immunology 2020Quote: ... Each well was mixed with 0.8 μl Nextera tagmentation DNA buffer (Illumina) and 0.4 μl Tn5 enzyme (Illumina) ...
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bioRxiv - Cancer Biology 2019Quote: ... Each well was mixed with 0.8 µl Nextera tagmentation DNA buffer (Illumina) and 0.4 µl Tn5 enzyme (Illumina) ...
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bioRxiv - Cell Biology 2023Quote: ... after which the plates were sequenced on the NextSeq 500 (Illumina) for 25 million reads per plate.
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bioRxiv - Genetics 2020Quote: ... Libraries were made according to the manufacturer’s directions for the TruSeq Stranded mRNA LT Sample Prep Kit – sets A and B (Illumina, Cat. No. RS-122-2101 and RS-122-2102). Resulting short fragment libraries were checked for quality and quantity using the Bioanalyzer (Agilent ...
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bioRxiv - Cancer Biology 2022Quote: ... ribosomal RNA depleted strand-specific RNA libraries with the TruSeq Stranded Total RNA LT sample preparation kit with Ribo-Zero Gold (Illumina, cat# RS-122-2301 and #RS-122-2302), and transcriptome capture based libraries with the TruSeq RNA Access Library Prep Kit (Illumina ...
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bioRxiv - Cancer Biology 2023Quote: ... ribosomal RNA depleted strand-specific RNA libraries with the TruSeq Stranded Total RNA LT sample preparation kit with Ribo-Zero Gold (Illumina, cat# RS-122-2301 and #RS-122-2302), and transcriptome capture based libraries with the TruSeq RNA Access Library Prep Kit (Illumina ...
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bioRxiv - Cell Biology 2020Quote: ... Libraries were diluted to 2 nM in each and pooled with equal volume before sequenced on Hiseq X Ten (Illumina, Inc., San Diego, CA, USA) with 150-bp pair-end strategies.
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bioRxiv - Developmental Biology 2021Quote: ... Sample libraries were sequenced on the NextSeq 500 (Illumina). Sequencing output was processed through the Cell Ranger 2.1.0 mkfastq and count pipelines using default parameters ...
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bioRxiv - Genomics 2021Quote: Dual indexed samples were demultiplexed using bcl2fastq software (Illumina). Subsequent data processing was carried out using specifically created scripts in Python ...
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bioRxiv - Developmental Biology 2021Quote: ... Sample de-multiplexing was performed using CASAVA 1.8.2 (Illumina).
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bioRxiv - Genetics 2019Quote: ... Samples were sequenced on a HiSeq 4000 platform (Illumina) with a Single End 50 run.
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bioRxiv - Microbiology 2019Quote: ... Those samples were then cleaned as recommended by Illumina, except that we started with 15 uL of amplified tagmented DNA and 12 μL of AMPure XP beads ...
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bioRxiv - Immunology 2019Quote: ... Samples were pooled and sequenced using the HiSeq2500 (Illumina) to obtain at least 12 million 50-bp single-end reads per library ...
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bioRxiv - Immunology 2019Quote: ... Samples were sequenced on NextSeq 500/500 sequencer (Illumina) with SE-85 ...
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bioRxiv - Immunology 2019Quote: ... Samples were de-multiplexed with bcl2fastq tool from Illumina, and tag bam files with read sequence extended were processed to differentiate molecular barcodes ...
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bioRxiv - Genomics 2021Quote: ... allocating 20M reads per sample (Illumina; single read sequencing). The RNA-Seq data ...
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bioRxiv - Neuroscience 2020Quote: ... An additional 5 samples were sequenced on MiSeq (Illumina).
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bioRxiv - Cancer Biology 2020Quote: ... pooled samples were sequenced using a NextSeq 500 (Illumina) and a High Output v2 ...
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bioRxiv - Synthetic Biology 2021Quote: ... The 100 PCR samples were then sequenced by Illumina sequencing platform ...
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bioRxiv - Microbiology 2021Quote: ... Samples were sequenced on a HiSeq 2500 system (Illumina) using single read (1×50 ...
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bioRxiv - Genomics 2021Quote: ... except for six samples that were processed by Illumina DNA Prep ...
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bioRxiv - Physiology 2021Quote: ... Samples were submitted to quality control (Illumina BioAnalyzer®) revealing the RNA integrity number (RIN ...
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bioRxiv - Genomics 2021Quote: ... The samples were sequenced on a HiSeq 2500 (Illumina) based on qPCR concentrations ...
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bioRxiv - Immunology 2021Quote: ... Samples were sequenced on NextSeq 500/500 sequencer (Illumina) with SE-85 ...
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bioRxiv - Cell Biology 2021Quote: ... Samples were used to construct Nextera XT libraries (Illumina) from 100 pg of preamplified cDNA ...
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bioRxiv - Cancer Biology 2021Quote: ... Sample processing through 10X Genomics and NextSeq 500 (Illumina) sequencing was performed by the Washington University Genome Technology Access Center (gtac.wustl.edu) ...
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bioRxiv - Microbiology 2022Quote: ... Multiplexed samples were then run on the MiSeq (Illumina). Adaptor sequences were automatically trimmed by the MiSeq platform and then raw reads were downloaded from basespace in FASTQ format ...
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bioRxiv - Genomics 2022Quote: Samples were demultiplexed using bcl2fastq 2.17.1.14 (Illumina, Inc., 2017). Quality checks were performed on the raw data using FastQC v0.11.8 (Andrews ...
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bioRxiv - Cancer Biology 2022Quote: ... Samples were sequenced on a MiSeq genome analyzer (Illumina). The sequencing reads were analyzed using CRISPResso2 (v.2.0.40 ...
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bioRxiv - Genetics 2020Quote: ... transcriptomes of 36 skin samples were obtained by Illumina sequencing (RNA-Seq).
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bioRxiv - Cell Biology 2021Quote: ... Samples were sequenced on the NextSeq 500 instrument (Illumina). Run data were demultiplexed and converted to fastq files using Illumina’s bcl2fastq Conversion Software version 2.18 on BaseSpace ...
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bioRxiv - Microbiology 2020Quote: ... Samples were sequenced on NextSeq or MiSeq system (Illumina) to produce 150 or 300 base-pair paired-end reads at the Bio-Genet NGS facility of Lyon University Hospital ...
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bioRxiv - Bioengineering 2020Quote: ... Samples were submitted for analysis on a HiSeq4000 (Illumina) with a custom primer ...
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bioRxiv - Genomics 2022Quote: ... Samples were sequenced on a NovaSeq 6000 system (Illumina) at a sequencing depth of minimum 50,000 reads per spot using a 100 cycles kit in paired-end mode ...
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bioRxiv - Bioengineering 2019Quote: ... Samples were analysed using the Infinium MethylationEPIC BeadChip (Illumina) according to the manufacturer’s instructions ...
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bioRxiv - Developmental Biology 2019Quote: ... Samples were sequenced using the HiSeq 4000 system (Illumina).
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bioRxiv - Genomics 2019Quote: The samples were sequenced on a HiSeq3000 instrument (Illumina) in 75 bp paired-end mode for the short libraries and in 150 bp paired-end mode for the medium and long libraries ...
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bioRxiv - Microbiology 2019Quote: ... and samples were sequenced on Illumina MiSeq (Illumina Inc.) to produce more than 100x coverage ...
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bioRxiv - Cancer Biology 2020Quote: ... Pooled sample libraries were sequenced on HiSeq 4000 (Illumina) sequencer to 50 bp single reads at ∼25-30 million read depth per sample ...
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bioRxiv - Cancer Biology 2020Quote: ... the samples were sequenced using Hiseq2500 sequencer (Illumina, USA). Trimmomatic processed the raw data and used featureCounts software to quantify the expression level of each gene ...
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bioRxiv - Molecular Biology 2021Quote: ... total RNA samples were treated with Ribo-Zero (Illumina) and used for RNA-seq library preparation using an Illumina TruSeq Stranded Total RNA Library Prep Kit (Illumina ...
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bioRxiv - Microbiology 2020Quote: ... Samples were sequenced on a NextSeq 550 instrument (Illumina) with 300 cycles (2 × 150 bp paired-end reads) ...
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bioRxiv - Genomics 2021Quote: ... The total RNA samples extracted were sequenced by Illumina NovaSeq6000 (Macrogen Japan Corp. ...
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Disruption of the TCA cycle reveals an ATF4-dependent integration of redox and amino acid metabolismbioRxiv - Biochemistry 2021Quote: ... The samples were run using NextSeq 500 sequencer (Illumina). Differential Gene Expression Analysis was done using the counted reads and the R package edgeR version 3.26.5 (R version 3.6.1 ...
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bioRxiv - Genetics 2021Quote: ... All samples were sequenced on the HiSeq platform (Illumina) using a 2×150 paired-end configuration.
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bioRxiv - Genetics 2020Quote: ... for a total of 323 samples sequenced by Illumina RNA-seq (Dubin et al ...
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bioRxiv - Microbiology 2021Quote: ... Samples were sequenced on NextSeq or MiSeq system (Illumina) to produce 150 or 300 base-pair paired-end reads at the Bio-Genet NGS facility of Lyon University Hospital ...
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bioRxiv - Cancer Biology 2019Quote: ... All samples were sequenced with the HiSeq 2500 (Illumina) technology according to standard protocols and with 8 million reads per sample.
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bioRxiv - Cancer Biology 2022Quote: ... and pooled samples sequenced on the HiSeq4000 platform (Illumina). Somatic and germline WES sequencing files were aligned to Hg38 using bwa (v0.7.17 ...