Labshake search
Citations for Illumina :
2701 - 2750 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 - Biophysics 2022Quote: ... to create 1 ml of a 20 pM denatured DNA sample (Illumina). PhiX control library (Illumina ...
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bioRxiv - Microbiology 2022Quote: ... Samples were sequenced with 250-bp reads on a MiSeq instrument (Illumina).
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bioRxiv - Microbiology 2022Quote: ... DNA samples were sequenced using the Illumina HiSeq X10 platform (Illumina, Inc) at the Wellcome Sanger Institute ...
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bioRxiv - Neuroscience 2021Quote: ... cDNA library samples were then sequenced with the HiSeq 4000 System (Illumina). For sample set 4 ...
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bioRxiv - Neuroscience 2019Quote: ... and sequenced 6 samples per lane on a HiSeq 2000 sequencer (Illumina) giving a depth of 30-35 million reads per sample.
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bioRxiv - Cancer Biology 2019Quote: ... 25 million reads per sample were sequenced on HiSeq 2500 sequencer (Illumina) in 50bp single read mode.
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bioRxiv - Cancer Biology 2020Quote: ... followed by enzymatic fragmentation and hybridization of the samples to BeadChips (Illumina). After a step of single-nucleotide extension ...
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bioRxiv - Cancer Biology 2021Quote: ... remission and relapse DNA samples from case LS01 were sequenced by Illumina UK and analysed using the remission sample as the matching normal ...
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bioRxiv - Evolutionary Biology 2022Quote: ... Hatchling (1dph) optic lobe samples were sequenced on a Novaseq6000 instrument (Illumina) using a 10% PhiX spike.
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bioRxiv - Microbiology 2022Quote: ... Samples were sequenced on a single lane on an Illumina HiSeq2500 (Illumina). Low-quality reads of resulting fastq files were removed using FastQC and trimmed using Trimmomatic (Quality >20 ...
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bioRxiv - Microbiology 2022Quote: ... Samples were demuxltiplexed using bcl2fastq v2.20 Conversion Software (Illumina, San Diego, CA). Sequencing reads were quantified with Salmon (Patro et al. ...
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bioRxiv - Immunology 2020Quote: ... Sequencing of the prepared samples was performed with a HiSeq2500 platform (Illumina). Data were analyzed with Long Ranger and visualized with Loupe (10X Genomics).
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bioRxiv - Evolutionary Biology 2019Quote: ... Samples were pooled and sequenced with the Hiseq® 2500 System (Illumina). Paired-end sequencing with 100 cycles for each side of the fragments was performed in one lane.
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bioRxiv - Molecular Biology 2019Quote: ... The samples were sequenced on a MiSeq or NextSeq 500 sequencer (Illumina).
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bioRxiv - Cell Biology 2020Quote: ... Samples were sequenced on an HiSeq 4000 instrument (Illumina, San Diego, CA).
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bioRxiv - Plant Biology 2020Quote: ... The RNA samples were then sequenced on the HiSeq 2000 platform (Illumina) by the Novogene Corporation ...
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bioRxiv - Molecular Biology 2021Quote: ... These samples were sequenced on the high-throughput sequencing platform (HiSeq2500, Illumina) using a 100 bp single-end strategy.
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bioRxiv - Cell Biology 2019Quote: ... Samples were pooled and run in single read 50 flow cell (Illumina) and run on a Hiseq 4000 (Illumina).
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bioRxiv - Molecular Biology 2019Quote: ... and samples were paired-end sequenced on the NextSeq 500 sequencer (Illumina) with a read length of 2 × 75 bp ...
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bioRxiv - Genomics 2019Quote: ... Samples were sequenced on an Illumina HiSeq 2500 (Illumina, San Diego, CA) at the Joint Genome Institute to generate 150bp paired-end reads ...
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bioRxiv - Genomics 2019Quote: ... Samples were sequenced on an Illumina HiSeq 2500 (Illumina, San Diego, CA) at the Joint Genome Institute to generate 51 bp single-end reads (Supplemental Table 2).
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bioRxiv - Genomics 2019Quote: ... Samples were sequenced on an Illumina HiSeq 2500 (Illumina, San Diego, CA) at the Joint Genome Institute to generate 150bp paired-end reads ...
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bioRxiv - Genomics 2021Quote: ... Samples were sequenced on a HiSeq 4000 sequencer (Illumina, San Diego, CA).
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bioRxiv - Genetics 2020Quote: ... we have utilized lin-41 DNA samples sequenced (Illumina single-end sequencing) from multiple generations from F2 to F5 of the same pool of animals treated with sgRNA guides “sg15 and sg16” ...
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bioRxiv - Neuroscience 2020Quote: ... All samples proceeded through Nextera XTDNA Library Preparation (Illumina FC-131-1096) using either Nextera XT Index Kit V2 Sets A-D (FC-131-2001 ...
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bioRxiv - Cell Biology 2021Quote: ... and barcoded reverse primers for each sample (NEBNext Index primers for Illumina). PCR products were purified using 1.8 volumes of Axygen AxyPrep magnetic beads (MAG-PCR-CL) ...
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bioRxiv - Genomics 2020Quote: ... We used the meta file to further filter the samples by Illumina technology ...
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bioRxiv - Cancer Biology 2020Quote: ... Single-cell ATAC-seq samples were sequenced on a NextSeq 500 (Illumina) instrument with 50 bp paired-end reads at the Centre for Health Genomics and Informatics (CHGI ...
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bioRxiv - Cancer Biology 2021Quote: ... FastQ files for each sample were obtained using bcl2fastq v2.20.0.422 software (Illumina). More than 6.5 M of pairs per sample were obtained ...
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bioRxiv - Cancer Biology 2022Quote: ... FastQ files for each sample were obtained using bcl2fastq 2.20 Software (Illumina). Differential expression analysis was performed with the Limma R package at the different time points (0 ...
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bioRxiv - Cancer Biology 2022Quote: ... FastQ files for each sample were obtained using CASAVA v1.8 software (Illumina). Differential expression between miR-28- and control-treated tumors was analyzed by ANOVA (314 protein coding transcripts ...
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bioRxiv - Developmental Biology 2022Quote: ... Small RNA-seq libraries samples were sequenced using a NextSeq 550 (Illumina) to obtain 79-nt ...
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bioRxiv - Genomics 2022Quote: ... Samples were sequenced 36 bp pair-end on the NextSeq 550 (Illumina) using the Illumina NextSeq 500/550 High Output Kit v2.5 (75 cycles ...
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bioRxiv - Genomics 2022Quote: ... we pooled the samples and sequenced them in a NovaSeq6000 S2 (Illumina) machine ...
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bioRxiv - Evolutionary Biology 2022Quote: ... Samples were separately tagged and sequenced on a HiSeq or NovaSeq (Illumina). We filtered read pairs that contained Illumina adaptor sequences with Trimmomatic v ...
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bioRxiv - Microbiology 2022Quote: ... All samples were pooled and sequenced using a NextSeq 500 sequencer (Illumina). After the sequencing reads were demultiplexed and preprocessed ...
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bioRxiv - Neuroscience 2022Quote: Samples were sequenced on the NextSeq 500 instrument (Illumina, San Diego, US) using a 38 paired end run ...
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bioRxiv - Immunology 2022Quote: ... Single-end sequencing was performed on HiSeq400 (Illumina, 200 million reads/sample). Raw sequencing reads were evaluated by FastQC (75) ...
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bioRxiv - Neuroscience 2022Quote: ... All samples proceeded through Nextera XTDNA Library Preparation (Illumina FC-131–1096) using either Nextera XT Index Kit V2 Sets A-D (FC-131–2001 ...
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bioRxiv - Plant Biology 2023Quote: ... Sample libraries were pooled equimolar and sequenced on a Novaseq 6000 (Illumina) with 150bp pair-end reads ...
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bioRxiv - Cancer Biology 2024Quote: ... FastQ files for each sample were obtained using CASAVA v1.8 software (Illumina). Reads were aligned to the Ensembl reference genome and converted to reads per gene with the STAR software.
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bioRxiv - Microbiology 2023Quote: ... After pooling the samples together in equimolar concentrations in resuspension buffer (Illumina), the MiniSeq denaturation protocol A (Illumina ...
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bioRxiv - Physiology 2024Quote: ... 100-bp forward strand reads per sample on NextSeq2000 (Illumina, CA, USA). DNA alignment ...
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bioRxiv - Immunology 2024Quote: ... Samples from each ROI were packaged into library for sequencing (NextSeq550, Illumina) following the procedure recommended by Nanostring ...
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bioRxiv - Molecular Biology 2024Quote: ... samples were sequenced on an Illumina® NovaSeq S4 (Illumina, California, USA) with a read length configuration of 150 PE for [188] M PE reads per sample (94M in each direction).
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bioRxiv - Microbiology 2024Quote: ... 16S rDNA amplicon samples were sequenced using Illumina MiSeq platform (Illumina Inc.). The raw data were analyzed according to our previous methods [24 ...
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bioRxiv - Genomics 2024Quote: ... followed by enzymatic fragmentation and application of the samples to BeadChips (Illumina). The arrays were fluorescently stained and scanned ...
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bioRxiv - Cancer Biology 2024Quote: ... All RNA-seq samples were sequenced paired-end on NovaSeq 6000 (Illumina).
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bioRxiv - Neuroscience 2023Quote: ... Samples were sequenced on the NextSeq 500 instrument (Illumina, San Diego, US) using a 43bp paired end run ...
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bioRxiv - Physiology 2023Quote: ... CLS138948) and samples were subjected to paired indexing sequencing (Illumina HiSeq 4000). RNA sequencing data were analysed using Seurat.