Labshake search
Citations for Illumina :
151 - 200 of 367 citations for cis Clopidogrel MP 13C d3 Derivative Pair of Enantiomers since 2020
Citations are collected from bioRxiv only, the total number of publications could be much larger.
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bioRxiv - Evolutionary Biology 2021Quote: ... and the resulting library was subjected to pair-end sequencing with a Novaseq 6000 sequencer (Illumina) by Macrogen Japan ...
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bioRxiv - Molecular Biology 2023Quote: ... and subjected to pair-end sequencing (100 cycles: 2×50) on the Novaseq-6000 sequencer (Illumina) at the Genomic platform (Gustave Roussy ...
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bioRxiv - Molecular Biology 2023Quote: We designed two primer pools of 106 primer pairs with DesignStudio (Illumina, San Diego, CA, USA) to amplify PKD1 ...
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bioRxiv - Cancer Biology 2023Quote: ... according to the manufacturer’s instructions and underwent 2 × 151 base-pair sequencing on Hiseq 4000 (Illumina) sequencers ...
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bioRxiv - Zoology 2022Quote: ... Fish were sequenced for 100 base pair reads on one lane of a NovaSeq 6000 (Illumina). A mean of 98.3 million (± 38.9 million standard deviation (s.d.) ...
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bioRxiv - Cancer Biology 2024Quote: ... The PCR product was sequenced using a paired-end 75 base pair (bp) reads protocol (Illumina).
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bioRxiv - Molecular Biology 2024Quote: ... Pair-end sequencing (2x300) was done with MiSeq Reagent Kit v3 in a MiSeq platform (Illumina) by following the manufacturer’s instructions.
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bioRxiv - Molecular Biology 2024Quote: ... and sequenced as 125- or 250-base-pair paired end reads using Illumina Hiseq 2500 (Illumina). WGBS data were deposited under the GEO accession number GSE252760.
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bioRxiv - Immunology 2024Quote: ... and were sequenced in pair-end mode using the NovaSeq 6000 S2 100 cycle kit (Illumina) targeting a depth of 25,000 reads per cell.
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bioRxiv - Microbiology 2024Quote: ... Libraries were pooled and run as 75 cycle pair end reads on a NextSeq 550 (Illumina) using a high output flow cell.
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bioRxiv - Genomics 2024Quote: ... pair-end sequencing (2*150) of each sample was performed on an Illumina platform (Illumina, USA).
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bioRxiv - Neuroscience 2024Quote: ... Samples were then multiplexed and 75 bp pair end reads were generated on a Nextseq500 (Illumina). After reads were trimmed for NEBNext Ultra II DNA (TruSeq ...
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bioRxiv - Physiology 2024Quote: ... Samples were multiplexed and sequenced in pairs on an Illumina Novaseq X (Illumina, San Diego, CA). The sequenced data were processed into expression matrices with the Cell Ranger Single-cell software 9.0.0 obtained at the following website (https://www.10xgenomics.com/support/software/cell-ranger/latest/release-notes/cr-release-notes) ...
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bioRxiv - Systems Biology 2024Quote: ... Demultiplexing of the data by sample using the defined index pairs was performed automatically by Illumina BaseSpace.
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bioRxiv - Genetics 2020Quote: The phage L cI−40 13−am43 genome was sequenced at New England Biolabs by combining data from Illumina and PacBio RS2 methods ...
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bioRxiv - Cell Biology 2020Quote: ... The resulting libraries were paired-end sequenced to >50 million read pairs on a HiSeq4000 platform (Illumina). Transcript quantification was performed using Kallisto v0.44.066 ...
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bioRxiv - Genomics 2020Quote: ... and were paired-end sequenced to at least 50 million read pairs on a HiSeq4000 platform (Illumina). Raw reads were mapped to the human reference genome (hg19 ...
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bioRxiv - Microbiology 2020Quote: ... DNA pair-ended library was performed according to Illumina’s Multiplexing Sample Preparation Guide (Illumina, San Diego, CA), the DNA was fragmented ...
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bioRxiv - Genomics 2022Quote: ... Approximately 200 million of 150 bases pair-end reads were generated using the HiSeq X System (Illumina). Raw Illumina reads were filtered by discarding read pairs if (1 ...
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bioRxiv - Microbiology 2020Quote: ... Libraries were sequenced by 150 base pair paired-end sequencing on a NovaSeq 6000 Sequencing System (Illumina). Assistance with quality control and next-generation sequencing was provided by the Vanderbilt Technologies for Advanced Genomics (VANTAGE ...
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bioRxiv - Immunology 2022Quote: ... pair-end 150 bp sequencing was used to generate high-quantity data (Illumina, San Diego, California, USA). Then ...
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bioRxiv - Plant Biology 2020Quote: ... Multiplexed libraries were sequenced with 2×150 base pairs paired-end reads on an HiSeq3000 instrument (Illumina).
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bioRxiv - Genomics 2021Quote: ... 11 kb and 13 kb) were prepared following Nextera protocol (Nextera Mate Pair sample preparation kit, Illumina). Each library was sequenced using 100 base-length read chemistry on a paired-end flow cell on the Illumina HiSeq2000 (Illumina ...
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bioRxiv - Genomics 2021Quote: ... and then used to create two pair-end libraries using a TruSeq DNA Sample Preparation Kit (Illumina) with insert sizes of ∼250 and ∼800 bp [Supplementary Table 3] ...
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bioRxiv - Microbiology 2022Quote: ... Mate-pair sequencing was carried out for 150 cycles using the Nextseq550 system (Illumina Inc., CA, USA) according to the manufacturer’s specifications ...
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bioRxiv - Molecular Biology 2023Quote: Exome sequencing of a sibling pair with generalized OA at multiple joint sites was performed by Illumina HiSeq 2000 technology (Beijing Genome Institute ...
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bioRxiv - Genomics 2023Quote: ... The resulting libraries were paired-end sequenced to >50 million read pairs on a HiSeq4000 platform (Illumina). Reads were trimmed and mapped to human genome hg19 using STAR ...
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bioRxiv - Developmental Biology 2024Quote: ... and subsequently sequenced on a NextSeq 500 sequencer (paired-end 43 base pairs) (Illumina, San Diego, CA) in a single run to reduce potential batch effects ...
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bioRxiv - Genomics 2022Quote: ... WGS of tumor-normal pairs was performed on the HiSeq X-Ten platform (Illumina, San Diego, USA), yielding paired-end reads of 2×150 bp length ...
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bioRxiv - Genetics 2022Quote: ... PCR amplicons were subjected to 300 pair-end read sequencing using Illumina MiSeq (Illumina, San Diego, CA). The detailed methods are described in Supplemental methods.
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bioRxiv - Immunology 2023Quote: ... Indexed samples were sequenced using a 150 base pair paired-end protocol via the HiSeq 2500 (Illumina) according to the manufacturer’s protocol ...
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bioRxiv - Molecular Biology 2024Quote: ... Diluted libraries were clustered on a pair-read flowcell and sequenced using a NovaSeq 6000 system (Illumina) (using «Genetiсo» facility).
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bioRxiv - Microbiology 2020Quote: ... and used the most contiguous assemblies (Oxford Nanopore – Illumina for D1,D2,D4,D6,D7,D8 and Pacbio Sequel – Illumina for D3,D5, RE1, RE2, RE3). Manual curation involved removing contigs smaller than 1kB ...
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bioRxiv - Microbiology 2020Quote: ... For the HiSeq cohort DNA libraries were pair-end sequenced using the HiSeq4000 high throughput sequencing platform (Illumina) in 2×150 bp ...
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bioRxiv - Immunology 2021Quote: ... Library preparation and RNA-seq libraries were prepared and RNA-seq (150-bp pair-end, NovaSeq 6000 Illumina) was done at the University of Minnesota Genomics Center ...
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bioRxiv - Microbiology 2021Quote: ... Libraries were then multiplexed and submitted to the sequencing platform (Illumina MiSeq, pair end 2 x 250 bp). Reads with less than 36 bp were discarded and adaptor sequences were removed by Macrogen Inc.
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bioRxiv - Cancer Biology 2020Quote: ... the library was performed pair-end 2×100bp high-throughput sequencing using HiSeq 2500 and Nova-seq (Illumina).
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bioRxiv - Microbiology 2020Quote: ... The pair-end sequencing library was prepared using the TruSeq DNA PCR-Free Prep Kit (Illumina, United States). The prepared library was sequenced on the NovaSeq 6000 platform (2 × 150 bp chemistry ...
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bioRxiv - Plant Biology 2022Quote: ... The library from each genotype was indexed using Unique Dual Index Primer Pairs (NEBNext Multiplex Oligos for Illumina) in order to perform multiplexed sequencing.
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bioRxiv - Physiology 2022Quote: ... The 30 fish were sequenced for 100 base pair reads on one lane of a NovaSeq 6000 (Illumina). A mean of 50.5 million reads per sample were sequenced (±9.2 million standard deviation ...
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bioRxiv - Neuroscience 2021Quote: ... and high-throughput sequencing was carried out using a HiSeq4,000 (2×75-base-pair paired-end configuration; Illumina). Bioinformatics analyses were performed as described (52)
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bioRxiv - Neuroscience 2021Quote: ... and high-throughput sequencing was carried out using a HiSeq4,000 (2×75-base-pair paired-end configuration; Illumina). Bioinformatics analyses were performed as described (47).
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bioRxiv - Genomics 2021Quote: ... Libraries were multiplexed and 150 base pair paired-end reads were generated on the HiSeq 4000 platform (Illumina). Samples with greater than approximately 300 ng remaining mass and a peak fragment length of greater than 19,000 bp (with minimal mass under 4,000 bp ...
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bioRxiv - Evolutionary Biology 2021Quote: Illumina sequencing reads (248,820,547 2x150 base pair (bp) paired-end reads) were demultiplexed into individual sample fastq files with the software bcl2fastq2 (v2.20.0, Illumina). The FastQC software [59] was used for visual inspection of read quality ...
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bioRxiv - Genomics 2021Quote: ... 89.5 Gb (~66× depth) Illumina HiSeq PE150 pair-end sequencing to correct errors (Illumina, San Diego, CA, USA); and (3 ...
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bioRxiv - Microbiology 2023Quote: ... they were sequenced on the Illumina NovaSeq-6000 platform to provide 250 bp (base pairs) paired reads (Illumina).
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bioRxiv - Genomics 2023Quote: ... Samples were multiplexed and sequenced with 2×75 bp pair-end reads on a NextSeq 500 instrument (Illumina).
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bioRxiv - Plant Biology 2023Quote: ... Sequencing libraries were prepared and 150 bp pair-end reads were sequenced using Illumina NovaSeq 6000 platform (Illumina) by Novogene.
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bioRxiv - Genomics 2023Quote: ... The constructed Hi-C sequencing library was first subjected to a test run of sequencing to evaluate valid interaction read pairs using HiCPro (v3.1.0) (Servant et al., 2015) before high coverage sequencing by Illumina NovaSeq 6000 to yield 705 Gb (∼138× genome coverage ...
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bioRxiv - Microbiology 2022Quote: ... The cleaned pool was sequenced on the Illumina MiSeq using v.2 2_250 base-pair kit (Illumina, Inc). Two PCR controls were also sequenced to test for PCR reagent contamination.