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Comprehensive determination of transcription start sites derived from all RNA polymerases using ReCappable-seq.
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capCLIP: a new tool to probe translational control in human cells through capture and identification of the eIF4E-mRNA interactome.
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Primer Extension Enrichment Reaction (PEER): A New Subtraction Method for Identification of Genetic Differences Between Biological Specimens
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MAPCap allows high-resolution detection and differential expression analysis of transcription start sites.
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5' RACE by tailing a general template-switching oligonucleotide.
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Reverse transcriptase template switching: a SMART approach for full-length cDNA library construction.
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Cloning of the human cDNA for the U1 RNA-associated 70K protein.
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Purifying mRNAs with a high-affinity eIF4E mutant identifies the short 3' poly(A) end phenotype.
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RNA captor: a tool for RNA characterization.
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NanoPARE: parallel analysis of RNA 5' ends from low-input RNA.
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An improved PCR method for walking in uncloned genomic DNA.
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Highly efficient subtractive hybridization of cDNA
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STRT-seq-2i: dual-index 5' single cell and nucleus RNA-seq on an addressable microwell array.
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A new method to prevent carry-over contaminations in two-step PCR NGS library preparations.
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Distinct populations of primary and secondary effectors during RNAi in C. elegans.
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Global amplification of cDNA from limiting amounts of tissue. An improved method for gene cloning and analysis
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Optimizing T4 DNA polymerase conditions enhances the efficiency of one-step sequence- and ligation-independent cloning.
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Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides.
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Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library.
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Oligodeoxyribonucleotide ligation to single-stranded cDNAs: a new tool for cloning 5' ends of mRNAs and for constructing cDNA libraries by in vitro amplification.
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5' Long serial analysis of gene expression (LongSAGE) and 3' LongSAGE for transcriptome characterization and genome annotation.
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Increasing the efficiency of SAGE adaptor ligation by directed ligation chemistry.
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Genome-wide identification of DNaseI hypersensitive sites using active chromatin sequence libraries.
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A simple and efficient method for direct cloning of PCR products using ddT-tailed vectors.
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The use of coded PCR primers enables high-throughput sequencing of multiple homolog amplification products by 454 parallel sequencing.
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cDNA library construction from a small amount of RNA: adaptor-ligation approach for two-round cRNA amplification using T7 and SP6 RNA polymerases.
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1274 full-open reading frames of transcripts expressed in the developing mouse nervous system.
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Identification of cell-specific messenger ribonucleic acids in oxytocinergic and vasopressinergic magnocellular neurons in rat supraoptic nucleus by single-cell differential hybridization.
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Gene discovery in genetically labeled single dopaminergic neurons of the retina.
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An efficient strategy to isolate full-length cDNAs based on an mRNA cap retention procedure (CAPture).
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A method for high-throughput production of sequence-verified DNA libraries and strain collections.
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Non-biased and efficient global amplification of a single-cell cDNA library.
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Extra-long first-strand cDNA synthesis.
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Reverse transcription using random pentadecamer primers increases yield and quality of resulting cDNA.
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Screening of genes associated with termination of the critical period of visual cortex plasticity in rats.
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Experimental discovery of sRNAs in Vibrio cholerae by direct cloning, 5S/tRNA depletion and parallel sequencing.
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Massive transcriptional start site analysis of human genes in hypoxia cells.
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A library-based method to rapidly analyse chromatin accessibility at multiple genomic regions.
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Construction of T-vectors, a rapid and general system for direct cloning of unmodified PCR products.
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Reduction of non-insert sequence reads by dimer eliminator LNA oligonucleotide for small RNA deep sequencing.
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Method for improving heat stability of RNA.
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