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Citations for Illumina :
1 - 50 of 606 citations for Breast Cancer Type 1 Susceptibility Protein BRCA1 Antibody since 2019
Citations are collected from bioRxiv only, the total number of publications could be much larger.
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bioRxiv - Cancer Biology 2021Quote: cDNA from tonsil and breast cancer tissue microregion samples were prepared into sequencing libraries using Nextera XT library preparation (Illumina), while cDNA from melanoma microregion libraries were prepared with ThruPLEX DNA-seq Kit (Takara Bio) ...
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bioRxiv - Genomics 2022Quote: ... California and Uganda Prostate Cancer Study (1590 cases/1048 controls on Illumina H3Africa consortium array ...
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bioRxiv - Genomics 2019Quote: ... nine whole-genome datasets from Japanese lung cancer patients (150PE, Illumina NovaSeq), 514 whole-exome datasets from TCGA-LUAD and 97 whole-exome datasets from Japanese lung adenocarcinoma patients (JGAS00000000001 ...
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bioRxiv - Genomics 2019Quote: ... 5 whole-genome datasets from cancer cell lines (DRA001859; 101PE, Illumina HiSeq2500), nine whole-genome datasets from Japanese lung cancer patients (150PE ...
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bioRxiv - Cancer Biology 2021Quote: ... and libraries were prepared using AmpliSeq Cancer HotSpot Panel v2 kit (Illumina). This panel targets 2800 COSMIC mutations in 50 oncogenes and tumor-suppressor genes ...
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bioRxiv - Cancer Biology 2020Quote: ... Sequencing was performed at Tisch Cancer Institute sequencing core on the NextSeq500 (Illumina) for 38 nucleotides each from paired ends according to manufacturer’s instructions.
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bioRxiv - Developmental Biology 2023Quote: ... Libraries 1-3 (wild type) were sequenced on a NovaSeq 6000 (Illumina) and the mutant library was sequenced on a NextSeq 500 (Illumina) ...
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bioRxiv - Microbiology 2019Quote: ... baumannii datasets were selected based on the availability of isolates collected during a single survey that were tested for CIP susceptibility and whole genome sequenced using consistent platforms (in both cases, the BD-Phoenix system and either Illumina MiSeq or NextSeq).
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bioRxiv - Microbiology 2021Quote: ... (Canada) (Sequencing type: Illumina NovaSeq 6000 S4 PE100 - 25M reads ...
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bioRxiv - Molecular Biology 2022Quote: ... Illumina array type (Illumina Infinium MethylationEPIC or Methylation450K BeadChip) ...
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bioRxiv - Cancer Biology 2023Quote: ... The mutational profile of GSCs was assessed using the TruSight Oncology 500 cancer panel (Illumina) and a NovaSeq 6000 instrument ...
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bioRxiv - Genomics 2020Quote: Library preparation for NGS sequencing was performed using TruSight RNA Pan-Cancer Panel (Illumina, SanDiego, CA, USA) targeting 1385 genes involved in cancer biology ...
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bioRxiv - Cell Biology 2021Quote: ... Sequencing was run at the Cancer Research UK Cambridge Institute Genomics core on a Novaseq 6000 (Illumina), using 50bp paired-end reads ...
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bioRxiv - Cancer Biology 2023Quote: ... We used the pan-cancer batch-corrected normalized gene expression and beta values for methylation from Illumina’s HumanMethylation450 BeadChip ...
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bioRxiv - Cancer Biology 2023Quote: ... Libraries were generated using TruSight Rapid Capture kit in combination with the TruSight Cancer Sequencing Panel (Illumina) according to the manufacturer’s protocol ...
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bioRxiv - Pathology 2020Quote: ... Enrichment and library preparation were performed with the TruSight Cancer Sequencing Panel v1 (Illumina, Inc., San Diego, USA) using 500ng of genomic DNA ...
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bioRxiv - Cancer Biology 2019Quote: ... We pre-compiled a gene panel that lists all prostate cancer-related genes (with the help of Illumina). By comparing with this panel ...
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bioRxiv - Immunology 2022Quote: ... mRNA purified from cancer cells was used for library construction with TruSeq RNA Sample Prep Kit v2 (Illumina) following the manufacturer’s instructions ...
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bioRxiv - Evolutionary Biology 2022Quote: ... Libraries were transported to the Cancer Research UK Genomics Core Facility and sequenced on NovaSeq 6000 system (Illumina).
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bioRxiv - Molecular Biology 2023Quote: ... We loaded the cancer patient samples on one lane of a NovaSeq 6000 (Illumina, San Diego, CA, USA) instrument at a concentration of 300 pM with 10% PhiX using the NovaSeq 6000 SP Reagent Kit v1.5 (100 cycles ...
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bioRxiv - Cancer Biology 2023Quote: We generated RNA-seq data from the H1299 non-small cell lung cancer cell line with 108,321,106 reads (TrueSeq RNA v2 100 bp paired-end library and Illumina HiSeq2500 machine from Illumina ...
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bioRxiv - Cancer Biology 2023Quote: ... NGS was performed at the Tumour Profiling Unit of the Institute of Cancer Research using NovaSeq 6000 (Illumina). 150 pair-end reads and 15% of PhiX was considered and approximately 5000 reads per time-point was aimed.
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bioRxiv - Genomics 2020Quote: Three types of sequencing reads from Illumina, PacBio ...
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bioRxiv - Cancer Biology 2021Quote: ... 2019) that including normal tissue sampled adjacent to colorectal cancers that was profiled using the HumanMethylation450 BeadChip array (Illumina).
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IRF1 regulates self-renewal and stress-responsiveness to support hematopoietic stem cell maintenancebioRxiv - Cell Biology 2023Quote: ... Sequencing was performed using Nova Seq S4 (run type: PE100, type of library: NexteraXT, 25 million reads per sample; Illumina). Preprocessing and analysis were done using Galaxy Quality and adapter trimming of reads was performed using RNA Galaxy workbench 2.058 ...
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bioRxiv - Cell Biology 2020Quote: ... Totally 3 μg of total RNA was ligated with 5′- and a 3′-adaptors sequentially with TruSeqTM Small RNA (or Stranded Total RNA in the case of cancer cells) Sample Prep Kit (Illumina). Briefly ...
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bioRxiv - Systems Biology 2020Quote: We applied PROB to a dataset of bladder cancer patients that includes 84 cases of conventional UCs and 28 cases of SARCs which were profiled by Illumina HumanHT-12 DASL Expression BeadChips (GSE128192 [39]) ...
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bioRxiv - Cancer Biology 2021Quote: ... Epigenomic studies were performed at the International Agency for Research on Cancer (IARC) with the Infinium EPIC DNA methylation beadchip platform (Illumina) used for the interrogation of over 850,000 CpG sites (dinucleotides that are the main target for methylation) ...
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bioRxiv - Cancer Biology 2022Quote: ... resistant and P12 cells of cell lines #3 and #9 was performed at the Genomics and Proteomics Core Facility of the German Cancer Research Center (GPCF DKFZ, Heidelberg) using the TruSeq DNA PCR-free Methyl protocol (Illumina) for library preparation ...
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bioRxiv - Genomics 2021Quote: ... RNA libraries were prepared for sequencing by the Cancer Genomics Shared Resource (Wake Forest School of Medicine, Winston-Salem, NC) using the TruSeq-stranded total RNA kit (Illumina), which includes a ribosomal depletion step ...
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bioRxiv - Developmental Biology 2022Quote: ... RNA was submitted to the Fred Hutchinson Cancer Research Center Genomics Core for library preparation using the TruSeq3 Stranded mRNA kit (Illumina) followed by size and quality analysis by Tapestation (Agilent) ...
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bioRxiv - Molecular Biology 2023Quote: Nuclei were submitted to the Cancer Research UK (CRUK) Cambridge Institute for 10x library preparation using V3 chemistry and sequencing on a NovaSeq 6000 (Illumina).
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bioRxiv - Developmental Biology 2023Quote: ... Samples were submitted to the Ohio State University Cancer Center Genomics Shared Resource for poly(A) selection and library preparation with TruSeq (Illumina) and subsequently sequenced on a HiSeq4000 (Illumina ...
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bioRxiv - Genomics 2022Quote: Combined with four types of libraries constructed: (1) the short-read sequencing library with 350-bp insertions from Illumina HiSeq X Ten instrument platforms ...
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bioRxiv - Developmental Biology 2022Quote: ... Libraries were generated at the Huntsman Cancer Institute Genomic Core facility using TruSeq Stranded Total RNA Library Prep with Ribo-Zero Gold kits (Illumina 20020598) and sequenced using the Illumina NovaSeq 6000 for 100M 2×50bp reads ...
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bioRxiv - Molecular Biology 2021Quote: Pooled equimolar libraries were sequenced at Canada’s Michael Smith Genome Sciences Centre (BC Cancer Research, Vancouver, BC, Canada, https://www.bcgsc.ca) using the Illumina Hiseq (Illumina Inc., San Diego, CA). The libraries were sequenced as a 150 bp paired end run ...
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bioRxiv - Plant Biology 2021Quote: ... biological replicates for each of eleven tissue types from Illumina mRNA-seq libraries were aligned independently using STAR v2.5.3a (Dobin et al. ...
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bioRxiv - Cancer Biology 2020Quote: ... is a 30-gene NGS test for somatic mutations in myeloid neoplasms using the Truseq Amplicon Cancer Panel kit (Illumina, San Diego, CA). It contains amplicons for hot-spot locations of the following genes ...
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bioRxiv - Genetics 2019Quote: ... DNA was submitted to the Huntsman Cancer Institute High Throughput genomic core for sequencing on a Hi-Seq 2500 (Illumina, San Diego, CA) using 50 cycle-single read chemistry ...
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bioRxiv - Immunology 2022Quote: ... Multiplexed samples were then sequenced at the Molecular Biology Core Facility (Dana-Farber Cancer Institute) and/or The Genomics Platform (Broad Institute) using an Illumina NextSeq 500 (Illumina, San Diego, CA), allowing 4×108 individual reads per multiplexed sample.
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bioRxiv - Neuroscience 2022Quote: ... Libraries were sequenced at Canada’s Michael Smith Genome Sciences Centre (BC Cancer Research, Vancouver, BC, Canada) using the Illumina HiseqX (Illumina Inc., San Diego, CA). On average ...
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bioRxiv - Genomics 2021Quote: ... libraries with an average insert size of 450 bp were prepared by the University of Utah’s Huntsman Cancer Institute High-Throughput Genomics Core Facility using the Illumina TruSeq DNA PCR-Free Library Prep Kit (Illumina, San Diego, California, USA). 2 × 150 bp reads for each parent were generated on an Illumina NovaSeq 6000 instrument using the NovaSeq S2 reagent kit (Illumina ...
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bioRxiv - Immunology 2024Quote: ... were prepared in the Fred Hutchinson Cancer Center (FHCC) Genomics Core Facility (Seattle, WA) using the TruSeq RNA Sample Prep Kit v2 (Illumina, San Diego, CA, USA), as previously described (Rose et al. ...
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bioRxiv - Microbiology 2021Quote: ... A draft wild type phi47 genome was assembled de novo from Illumina reads obtained from MiGS ...
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bioRxiv - Developmental Biology 2023Quote: ... Both types of arrays were scanned on a NextSeq 550 system (Illumina). HMW genomic DNA was sequenced to ∼30x coverage on a NovaSeq 6000 (Illumina) ...
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bioRxiv - Genomics 2020Quote: ... The first type consists of Labyrinthula transcripts generated in this study by sequencing (Illumina) and assembling the transcriptome (Haas et al ...
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bioRxiv - Genetics 2022Quote: DMDSC genotyping was conducted for approximately 5,801 patients with type 2 diabetes by Illumina using the global screening arrays version (GSA v1.0) ...
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Alzheimer’s patient brain myeloid cells exhibit enhanced aging and unique transcriptional activationbioRxiv - Neuroscience 2019Quote: ... The libraries were multiplexed within cell types and then sequenced on Illumina HiSeq2500 (Illumina) to generate 50M of single end 50bp reads.
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bioRxiv - Genomics 2021Quote: ... HLA types were further confirmed with ImmunoArray-24 BeadChip v2.0 (Infinium) or HumanImmuno BeadChip v1.0 (Illumina) and HLA imputation [36] ...
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bioRxiv - Genomics 2020Quote: ... Libraries for each sample type were prepared using the TruSeq Stranded Total RNA Library Prep Kit (Illumina), multiplexed and 75 bp paired-end sequenced over 4 lanes on an Illumina NextSeq 500 Sequencing System at the sequencing core facility at LANGEBIO ...