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Citations for Illumina :
1 - 50 of 69 citations for Acyl CoA Dehydrogenase Very Long Chain ACADVL Antibody since 2019
Citations are collected from bioRxiv only, the total number of publications could be much larger.
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bioRxiv - Genetics 2021Quote: ... Unanchored contigs shorter than 40kb were removed (considered as likely contaminants as very few Illumina reads were mapped on these short contigs).
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bioRxiv - Synthetic Biology 2023Quote: ... short-and long-read sequencing (Illumina and Oxford Nanopore technologies [ONT] ...
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bioRxiv - Microbiology 2023Quote: Short and long reads from Illumina and ONT sequencing ...
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bioRxiv - Cancer Biology 2021Quote: Long read ChIA-PET was performed using Tn5 transposase to tag DNA for long tag sequencing by Illumina NextSeq ...
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bioRxiv - Microbiology 2021Quote: Short and long reads generated by Illumina and Nanopore sequencing ...
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bioRxiv - Microbiology 2020Quote: ... Hyperlinks to the long (Nanopore) and short (Illumina) sequence reads at the Sequence Read Archive or MG-RAST database are provided in Table 1 and Tables S7 and S13 of Supplementary information.
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bioRxiv - Evolutionary Biology 2020Quote: ... We found 41 SNPs in the strain MvSn-1249-A2 (the very same fungal strain as the reference genome also sequenced with Illumina), indicating low rates of false positives in our SNP calling ...
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bioRxiv - Genomics 2019Quote: ... Synthetic long reads were generated by Moleculo (now Illumina) from barcoded libraries ...
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bioRxiv - Genomics 2019Quote: Long read (ONT nanopore reads) and short read (Illumina PE) WGS hybrid assembly.
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The effect of hybridization on transposable element accumulation in an undomesticated fungal speciesbioRxiv - Genomics 2020Quote: ... paradoxus strains using a combination of long (Oxford Nanopore) and short (Illumina) reads (PRJNA514804) ...
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bioRxiv - Genomics 2020Quote: ... Paired-end sequences of 150 bp long were determined using HiSeq X (Illumina). Approximately 1.8 billion sequence reads were obtained from each sample ...
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bioRxiv - Evolutionary Biology 2020Quote: ... were prepped and sequenced (paired-end 75bp-long reads) on HiSeq2500 V4 (Illumina) by and at the Sanger Sequencing Facility ...
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bioRxiv - Cell Biology 2021Quote: ... The corrected long-read sequences from MinION and short-read sequences from Illumina Miseq were hybrid de novo assembled using rnaSPAdes v3.14.1 (75)(https://cab.spbu.ru/software/rnaspades/ ...
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bioRxiv - Genomics 2020Quote: ... we first combined all sequence data (Illumina short reads and Nanopore long reads) in a hybrid assembly using MaSuRCA v3.4.2 [64] at –ploidy 2 using cabog in the final step of assembling corrected mega-reads.
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bioRxiv - Genomics 2020Quote: ... 201511 based on the Illumina Nextera Long Mate Pair Kit (Illumina, San Diego, USA). Sequencing was performed on Illumina HiSeq 2500 instruments with a 2×250 bp read metric targeting >60x raw coverage of the amplification-free library and 30x coverage of a combination of different insert long mate pair libraries with inserts sizes >7 kbp.
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bioRxiv - Plant Biology 2022Quote: ... corymbosa we used long reads from Oxford Nanopore sequencing and short reads from Illumina sequencing ...
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bioRxiv - Genomics 2023Quote: ... muscle and liver (Nanopore long reads and Illumina short reads, MNHN ZO-2020-125) or liver (Hi-C ...
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bioRxiv - Evolutionary Biology 2023Quote: ... and Proteles cristatus genomes have been previously reconstructed using long (ONT) and short (Illumina) reads assembled with MaSuRCA v3.2.9 (88 ...
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bioRxiv - Genomics 2021Quote: ... The single Unitig obtained by long-read sequencing was corrected with Mi-Seq (Illumina®) data using Pilon (version 1.21) ...
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bioRxiv - Cancer Biology 2020Quote: ... Sequencing of 75 nucleotide-long paired-end reads was performed in a NextSeq-500 (Illumina).
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bioRxiv - Cancer Biology 2020Quote: ... Sequencing of 75 nucleotide-long single-end reads was performed in a NextSeq-500 (Illumina).
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bioRxiv - Evolutionary Biology 2021Quote: ... 50 Kb long-read libraries were prepared using the 10X Genomics (Illumina Hiseq X Ten) platform ...
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bioRxiv - Genomics 2021Quote: ... The SLR library was constructed by a TruSeq synthetic long-read DNA library prep kit (Illumina), and sequences were generated by Illumina HiSeq 2000 and MiSeq systems with read lengths of 93nt and 251nt ...
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bioRxiv - Microbiology 2019Quote: The Lokiarchaeota MAGs obtained from hybrid assemblies using both short- and long-read metagenomics (Illumina and Nanopore) datasets are available via this link ...
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bioRxiv - Genomics 2022Quote: ... and manually cut when misassemblies were detected (i.e. regions with nonoverlapping long reads, mis-pairing of Illumina reads ...
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bioRxiv - Synthetic Biology 2023Quote: ... Long reads were produced using a GridION device (Oxford Nanopore) and short reads a MiSeq device (Illumina). For the Mcap cl12.1 transplant ...
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bioRxiv - Genomics 2021Quote: ... were prepped according to the manufacturer’s instructions and sequenced (paired-end 75bp-long reads) on HiSeq2500 V4 (Illumina) by the sequencing facility of the Wellcome Sanger Institute ...
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bioRxiv - Neuroscience 2020Quote: Long RNA libraries (mRNAs and lncRNAs) were prepared with the Illumina TruSeq Stranded RNA Library Prep (Illumina, USA). Sequencing (75 nts paired-end ...
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bioRxiv - Genomics 2024Quote: ... The ChIA-PET libraries were sequenced with 150 bps long paired-end reads using NovaSeq 6000 instrument (Illumina).
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bioRxiv - Plant Biology 2021Quote: A genetic linkage map of 2,110 cM long with an average distance of 0.92 cM was previously developed using the 90K iSelect SNP assay (Illumina) as described (Avni et al. ...
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bioRxiv - Genomics 2021Quote: ... (iii) and one TruSeq Synthetic Long-Read library were prepared according to the kit’s specifications and sequenced by Illumina sequencing technology ...
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bioRxiv - Genomics 2021Quote: ... The reads sequenced from the TruSeq Synthetic Long-Read library were assembled into long synthetic reads larger than 1.5 kb using the TruSeq Long-Read Assembly app v1.1 available on BaseSpace (Illumina Inc.).
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bioRxiv - Genetics 2021Quote: ... Loss of heterozygosity along the entire long arm of chromosome 15 in AS-UPD9 iPSCs was confirmed by Illumina CytoSNP-850K v1.2 array by the University of Connecticut Chromosome Core ...
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bioRxiv - Microbiology 2023Quote: ... and long range amplicons were used as input DNA for library preparation using the Nextera XT DNA Kit (Illumina) following the manufacturer’s protocol ...
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bioRxiv - Genomics 2022Quote: A complete genome sequence was generated combining SMRT long-read sequencing (Pacific Biosciences) and Illumina short-read sequencing (Illumina) as described in detail previously (Steglich et al. ...
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bioRxiv - Systems Biology 2023Quote: ... The final library was sequenced as 85 bp long single-end reads on a NextSeq™ 550 (Illumina, USA).
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bioRxiv - Genomics 2023Quote: Sequencing libraries were prepared using the TruSeq Synthetic Long-Read DNA Library Prep Kit (Illumina, Inc; San Diego CA). Three sequencing libraries were prepared by loading the sample into a Covaris g-TUBE (part no ...
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bioRxiv - Immunology 2022Quote: Single cell polymerase chain reaction (PCR) and custom molecular biology protocols generated NGS sequencing libraries (MiSeq, Illumina) using automated workstations (Bravo ...
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bioRxiv - Developmental Biology 2021Quote: ... Long mRNA libraries (2 replicates per time-point) were built using the TruSeq Stranded mRNA HT Sample Prep Kit (Illumina). Library concentration was assessed for all libraries using the Qubit fluorimetric system (Invitrogen ...
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bioRxiv - Molecular Biology 2020Quote: ... Half of the long RNA eluate was used to generate poly(A)+ libraries using the TruSeq Stranded mRNA Library Prep Kit (Illumina). The other half the long RNA eluate was used for total RNA library construction ...
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bioRxiv - Microbiology 2020Quote: Sequencing libraries were prepared for each product of long PCR (ranging from 15 to 33 kb) using the Nextera XT DNA Sample Preparation Kit (Illumina) and sequenced on the Illumina MiSeq platform to generate paired-end (PE ...
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bioRxiv - Genetics 2020Quote: ... Depletion of ribosomal RNA was performed on the short fractions and on half of the long fractions using a Ribo-zero rRNA removal kit (Illumina), according to the supplier’s instructions ...
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bioRxiv - Cancer Biology 2023Quote: ... RIN>6.8) was used for ribonucleotide-depleted long-noncoding RNA sequencing on a NovaSeq 6000 (Illumina, San Diego, CA, USA). Fastq reads were aligned to the human reference genome GRCh38 using STAR (version 2.6.0c ...
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bioRxiv - Microbiology 2023Quote: Long read sequencing using the Oxford Nanopore Platform (Long read DNA sequencing kit) and short read sequencing using the Illumina platform (Illumina DNA Prep kit and IDT 10bp UDI indices ...
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bioRxiv - Genomics 2021Quote: ... Purified DNA was subjected to both long-read (Nanopore GridION-X5 sequencer, Oxford Nanopore Technologies, Oxford, UK) and short-read (Illumina Technologies)
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bioRxiv - Genomics 2021Quote: ... Purified DNA was subjected to both long-read (Nanopore GridION-X5 sequencer, Oxford Nanopore Technologies, Oxford, UK) and short-read (Illumina sequencer) sequencing.
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bioRxiv - Immunology 2024Quote: Amplified IgG heavy- and light-chain variable regions were sequenced on an Illumina MiSeq (600-base v3 kit; Illumina) and reads corresponding to the same plate/well location were combined into consensus sequences ...
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bioRxiv - Genomics 2019Quote: ... 500bp and 800bp) and long insert mate-pair reads (4-6Kb, 8-10Kb and 1-20Kb) were sequenced using HiSeq 2500 (Illumina Inc., USA) at SciGenom Labs ...
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bioRxiv - Developmental Biology 2023Quote: ... Approximately 35 million pair-end sequences of 100 nucleotides long were produced per sample in a NovaSeq6000 instrument (Illumina, San Diego, CA) at the Genomics Technology Core at the University of Missouri.
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bioRxiv - Cancer Biology 2024Quote: ... is used to align long isoform reads to the reference genome hg38 (instead of the STAR aligner used with shorter Illumina RAN-seq), followed by our implementation of the GATK best practices for variant calling using RNA-seq (https://gatk.broadinstitute.org/hc/en-us/articles/360035531192-RNAseq-short-variant-discovery-SNPs-Indels) ...