Micromon in Clayton North, Victoria | Medical centre

Micromon

Locality: Clayton North, Victoria

Phone: +61 3 9905 8592

Address: 35 Rainforest Walk 3800 Clayton, VIC, Australia

Website: http://DNA.med.monash.edu.au

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• Medical and health
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25.01.2022 Here is a useful database of tools for a variety of -omics studies. Each area (genomics, proteomics, etc) is split into the methods (ChIP-seq, RNA-seq, etc), and from there there is a list of software packages available to analyse these datasets.

23.01.2022 The Human Cell Atlas project has been announced on biorxiv: "The goal of this article is to engage the wider scientific community in this conversation. We articulate the concept of a cell atlas and explore its potential utility for biology and medicine. We discuss how an atlas can lead to new understanding of histology, development, physiology, pathology, and intra- and inter-cellular regulation, and enhance our ability to predict the impact of perturbations on cells. It will also yield molecular tools with applications in both research and clinical practice. As discussed below, a Human Cell Atlas Project would be a shared international effort involving diverse scientific communities."

22.01.2022 Interested in learning or refreshing your skills in essential molecular biology? Sign up for the Micromon Recombinant DNA Techniques Course: 3-8 December.

21.01.2022 Phylogenetic trees: We see them all the time, but do you know how to read them? Here's a quick guide.

20.01.2022 Want to cut single-cell RNA-seq costs by multiplexing cell capture? Interested in simultaneous measurment of surface proteins & transcripts in single cells by sequencing? Join us for a seminar by Kathryn Friend from BioLegend. 18 April 2019, 10:30am, Physiology seminar room, 26 Innovation Walk, Monash University (Clayton Campus). #CITEseq #totalSeq #singleCell #scRNAseq #REAPseq

19.01.2022 Are you interested in 3-D genome conformation, epigenetics and genomic architecture? Join us for a seminar on Dovetail library construction technology. We're also announcing a discounted introductory offer!

19.01.2022 Getting Started with Single Cell ATAC Sequencing for High Resolution Epigenomic Studies Discover epigenetic heterogeneity at single cell resolution. Explore single cell ATAC-seq (Assay for Transposase-Accessible Chromatin using sequencing), an innovative approach to profile genome-wide, chromatin accessibility for hundreds to thousands of individual cells. Join an interactive, online webinar with 10x Genomics and learn experimental design, sample prep, and downstream data ana...lysis for single cell ATAC-seq. Speaker: Laura DeMare, Ph.D. Associate Product Manager, Epigenomics Tuesday, April 23 at 2:00 pm

19.01.2022 Replicates, Read Numbers, and Other Important Experimental Design Considerations for Microbial RNA-seq.

18.01.2022 Interested in single cell epigenomics and chromatin accessibility? Join the 10X "getting started" webinar, and visit us to talk about how you can get started! Getting Started with Single Cell ATAC Sequencing for High Resolution Epigenomic Studies: Discover epigenetic heterogeneity at single cell resolution. Explore single cell ATAC-seq (Assay for Transposase-Accessible Chromatin using sequencing), an innovative approach to profile genome-wide, chromatin accessibility for hund...reds to thousands of individual cells. Join an interactive, online workshop with 10x Genomics and learn experimental design, sample prep, and downstream data analysis for single cell ATAC-seq. The workshop will cover: - Expanding your research toolbox w scATAC-seq - How to generate scATAC-seq libraries - Best practices for sample preparation - Software and visualization tools

14.01.2022 Interested in single cell sequencing but not sure where to start? Need some help planning your experiment? Just want to see what it can do? 10X Genomics is hosting a regional "getting started" webinar, and we always here to help. Drop in and visit us for more information and a close-up look at the system!

12.01.2022 Micromon is moving! We're still at the Monash University Clayton Campus, but we're moving to 35 Rainforest Walk.

11.01.2022 Seminar: 10X Genomics and the Power of Linked Reads Presented by Deanna Church, 10X Genomics Hosted by Micromon and Millenium Science... Genomic Analysis - Discover What You Have Been Missing! 10x’s products enable a diverse set of sequencing applications, bringing unprecedented levels of depth to genomic analysis. The GemCode Technology uses the power of linked reads to fully resolve genic phasing, reveal structural variation, de novo genome assembly, remapping of difficult regions of the genome, and dynamic gene expression of single cells.The Chromium system from 10X Genomics is rapidly becoming the platform of choice for groups looking to single cell resolution of complex tissues or blood. Its ability to efficiently encapsulate from 100 10,000 cells per sample with high efficiency, consistency and reproducibility are hallmarks of this technology. This workshop will explain the technology, show how it is being used in cancer research and how it fits with other single cell platforms to deliver a comprehensive view of cellular heterogeneity.

10.01.2022 Seminar: 10X Genomics: A new technology for Single Cell Transcriptomics & Long-Range Genomics Joseph Aman, Senior Applications Scientist at 10X Genomics Room G19, 15 Innovation Walk (STRIP 1) Monash University, Clayton Campus... 10X Genomics, in collaboration with Millenium Science and Micromon, will present a seminar on the Chromium System which supports comprehensive genomics and high-throughput single cell transcriptomics with its innovative reagent delivery system. This technology, which is now available at Micromon (Monash University), enables the discovery of previously inaccessible genetic information at massive rate and scale (including phased structural variants, phased single nucleotide variants, and dynamic gene expression of individual cells). Contact us to book your place (RSVP required): [email protected] [email protected]

10.01.2022 Micromon is please to offer a huge end-of-year sale on next-generation sequencing... up to 50% off our standard list prices! * No maximum number of lanes/flowcells/samples * High per-lane yield (400m reads) * $1700/lane (PE100) or $2200/lane (PE150)... * No overseas shipping costs, delays or permits Contact us for a quote, or visit our webpage for more information! http://dna.med.monash.edu.au/index.php/news/92-salemainpage

10.01.2022 Having trouble with your library prep yield? Many library prep methods are very sensitive to inhibitors and, as a service provider, we often come across these issues in submitted samples. This technical note from illumina provides a brief introduction to the problem and offers some advice. If you suspect a problem, come and talk to us about what you can do about it, and how we can help!

09.01.2022 Here's a quick (and free) way to search the literature for methods...

07.01.2022 Do you carry out microbial transcriptomics? If so, please be aware that Illumina has discontinued all microbial Epicentre/Illumina ScriptSeq and RiboZero products (gram positive, gram negative, gold, epidemiology, etc), with very short notice and without replacement with an alternative product. Micromon will still provide microbial transcriptomics services, but we will use different technology to produce the sequencing libraries. Please contact us if you would like to discuss alternative options (if you prepare your own libraries) or implications of library chemistry changes (if you have obtained RNA-seq data from us in the past).

06.01.2022 10X Genomics' Chromium Controller. Changing the definition of sequencing. Now available at Micromon for high-throughput single cell transcriptomics, long-range genetic linkage information such as structural variation detection, phasing of structural variants, calling and phasing of SNPs, inversions, and deletions, de novo assembly, and more! Contact us for further information or to talk about how this technology might help your research projects.

06.01.2022 Join us tomorrow for a session on 10X Genomics' Chromium controller to see what it can do for your research. Single cell expression profiling, and also linked-read genome resolution, phasing and structural variation detection!

06.01.2022 We're looking forward to providing a variety of new single-cell applications via our 10X Chromium system: 1) single-cell ATAC-seq for chromatin accessibility, 2) Simultaneous cell surface protein abundance and transcriptome measurement, 3) CRISPR perturbation on the transcriptome per-cell, 4) Single-cell copy number analysis. The technology has been announced, and is expected to be available towards the end of the year. Contact us for further information!

05.01.2022 A review of epigenetics.

04.01.2022 We're excited to announce our newest sequencing platform, the MGISEQ-2000. It expands our sequencing throughput, decreases our large-project turn-around time and provides higher quality data! Perhaps most importantly, it allows us to provide sequencing data at fantastic prices... Contact us for a quote!

03.01.2022 Join us for our second Dovetail library construction webinar: Genome scaffolding with Dovetail Proximity Ligation Reads https://us02web.zoom.us//tZMscOChpzkuEtOUOe7I52B1LHMUSAzEL

02.01.2022 In an age of speed-optimised kits and automation, we're preparing DNA the old-fashioned way again! Using protocols from decades ago, we're spending almost a full day to prepare a single batch of samples using lots of cells, lots of phenol and chloroform, and collecting the DNA by spooling it onto a glass rod. Why are we doing this? We're aiming for ultra-long reads on our Nanopore sequencers! Almost all "modern" methods use spin columns or beads (SPRI or silica), which are qu...ick and convenient, but produce sheared DNA. Using phenol/chloroform and ethanol precipitation allows us to treat the DNA very gently, and to build sequencing libraries containing very long molecules. Unlike almost all other sequencing methods, the length of nanopore derived sequencing reads are limited only by the length of the DNA available to them. We're aiming for megabase reads! This length of read can potentially cover almost a whole microbial genome per read. The picture shows a tube of freshly precipitated bacterial genomic DNA, visible as long white threads in an acidified ethanol solution, ready for spooling and washing in more ethanol. See more