postdoc postdoctoral position NIH

We are at the National Institute of Child Health and Human Development (NICHD) at NIH. Our lab is interested in understanding cell lineage differentiation, gene regulation and how non-coding DNA elements and the 3D architecture of chromosomes contribute to these processes during early mouse development.

Learn more at pedrorochalab.org

What we offer:

  • Fully-funded postdoc positions up to five years including health benefits.
  • Opportunity to start your own research program or lead ongoing projects.

Who you are:

  • You share our enthusiasm for epigenetics, gene regulation, nuclear organization and mouse development.
  • You have PhD-experience in one or more of the following: mouse development, mouse genetics, epigenetics, massively-parallel sequencing techniques or computational biology.

Advantages of postdoctoral training at NIH

  • Fully-funded positions up to five years.
  • Large, diverse and extraordinary scientific network at the NIH/Bethesda campus. The NIH research community is unparalleled in its size, diversity and resources.
  • Possibility of living in a diverse, liberal and vibrant city: Washington DC
  • Or living in a calm residential area with great schools and good affordable housing, Bethesda and Rockville.
  • The NIH provides an invaluable resources for a wide array of postdoctoral training for career-growth.

Apply: 

Send the following to gsrunit@gmail.com:

  • 2 paragraph cover letter explaining your scientific trajectory and why you would like to join us.
  • CV and email contacts for 3 references.

The NIH is dedicated to building a diverse community in its training and employment programs.

post doc position at NIH
We combine imaging techniques in both fixed and living cells with sequencing- based genomic techniques that assess DNA-DNA interactions.
(A) Hi-C and CTCF ChIP- seq of GM1278 cells
(B) dCAS9 MCP-EGFP and PCP-CHERRY live imaging of the Igh and Akap6 loci.
The mouse embryo is an unparalleled system in mammalian biology for understanding how tissue- specific gene expression is achieved.
(C) Whole mount in-situ hybridization for patterning markers in mid and late gastrulating embryos.
(D) Tetraploid aggregation with GFP ES cells allows generation of fully ES-cell derived embryos.

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