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FISH_System_datafile_template.yaml
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# Automatic ROBOFISH info
# Make sure to always put a space between the colon and the value!
FISHSystem:
Parameters:
# Operator running the experiment. Same as name linked to Pushbulet code, lower case
Operator:
# Machine the experiment is run on: ROBOFISH1, ROBOFISH2 or NOT-DEFINED
Machine: ROBOFISH
########## EXPERIMENT 1 ##########
# Experiment name: Initials with date, like: LBEXP20181220_1
EXP_name_1:
# Short description of the Experiment
Description_1:
# Link to the protocol file on Protocols.io
Protocols_io_1:
# YYYYMMDD
Start_date_1:
# Chamber1 or Chamber2
Chamber_EXP_1: Chamber1
# First Hybridization time in hours (encoding probes)
Hyb_time_1_A:
# Second Hybridization time in hours (amplifier probes)
Hyb_time_1_B:
# Third Hybridization time in hours (detection probes)
Hyb_time_1_C:
# Experiment_type: smfish-serial, smfish-barcoded, eel-barcoded
Experiment_type_1:
# Total number of rounds
Target_cycles_1:
# True or False if a barcode is used
Barcode_1: true
# Name of the detection chemisty, like: EELV2_core, EELV2_all, indirect_64
Chemistry_1:
# Name of the codebooks
Codebook_DAPI_1:
Codebook_Atto425_1:
Codebook_FITC_1:
Codebook_Cy3_1:
Codebook_TxRed_1:
Codebook_Cy5_1:
Codebook_Cy7_1:
Codebook_Europium_1:
# True if there are multicolor barcodes
Multicolor_barcode_1: false
# Name of the FASTA file with the probe sequences
Probes_FASTA_DAPI_1:
Probes_FASTA_Atto425_1:
Probes_FASTA_FITC_1:
Probes_FASTA_Cy3_1:
Probes_FASTA_TxRed_1:
Probes_FASTA_Cy5_1:
Probes_FASTA_Cy7_1:
Probes_FASTA_Europium_1:
# Number of bits in the barcode
Barcode_length_1: 16
# Species:
Species_1:
# Strain of the animal
Strain_1:
# Sample identification number
Sample_1:
# Age of sample. Use letter indication for age system. Like: e for embryonic or ga for gestational age
Age_1:
# Tissue
Tissue_1:
# Section orientation
Orientation_1:
# Region imaged
RegionImaged_1:
# Section ID
SectionID_1:
# Coordinates of the section. (use appropriate coordinate system for species)
Position_1:
# Stiching type: small-beads, large-beads, both-beads, nuclei
Stitching_type_1:
# Channel to be used for stitching
StitchingChannel_1:
# Overlap percentage between fields of view
Overlapping_percentage_1:
# List of lists with coordinates of the roi's, like: [[0, 120], [121, 237]]
roi_1: [[0, 0]]
# Name of analysis pipeline to use. Options: eel-human-GBM, eel-human-adult-brain, eel-human-embryo
Pipeline_1:
########## EXPERIMENT 2 ##########
# Experiment name: Initials with date, like: LBEXP20181220_Mouse_2
EXP_name_2:
# Short description of the Experiment
Description_2:
# Link to the protocol file on Protocols.io
Protocols_io_2:
# YYYY-MM-DD HH:MM
Start_date_2:
# Chamber1 or Chamber2
Chamber_EXP_2:
# First Hybridization time in hours (encoding probes)
Hyb_time_2_A:
# Second Hybridization time in hours (amplifier probes)
Hyb_time_2_B:
# Third Hybridization time in hours (detection probes)
Hyb_time_2_C:
# Experiment_type: smfish-serial, smfish-barcoded
Experiment_type_2:
# Total number of rounds
Target_cycles_2:
# True or False if a barcode is used
Barcode_2:
# Name of the detection chemisty, like:
Chemistry_2:
# Name of the codebooks
Codebook_DAPI_2:
Codebook_Atto425_2:
Codebook_FITC_2:
Codebook_Cy3_2:
Codebook_TxRed_2:
Codebook_Cy5_2:
Codebook_Cy7_2:
Codebook_Europium_2:
# True if there are multicolor barcodes
Multicolor_barcode_2: false
# Name of the FASTA file with the probe sequences
Probes_FASTA_DAPI_2:
Probes_FASTA_Atto425_2:
Probes_FASTA_FITC_2:
Probes_FASTA_Cy3_2:
Probes_FASTA_TxRed_2:
Probes_FASTA_Cy5_2:
Probes_FASTA_Cy7_2:
Probes_FASTA_Europium_2:
# Number of bits in the barcode
Barcode_length_2:
# Species:
Species_2:
# Strain of the animal
Strain_2:
# Sample identification number
Sample_2:
# Age of sample. Use letter indication for age system. Like: e for embryonic or ga for gestational age
Age_2:
# Tissue
Tissue_2:
# Section orientation
Orientation_2:
# Region imaged
RegionImaged_2:
# Section ID
SectionID_2:
# Coordinates of the section. (use appropriate coordinate system for species)
Position_2:
# Stiching type: small-beads, large-beads, nuclei
Stitching_type_2:
# Channel to be used for stitching
StitchingChannel_2:
# Overlap percentage between fields of view
Overlapping_percentage_2:
# List of lists with coordinates of the roi's, like: [[1, 120], [121, 237]]
roi_2: [[0, 0]]
# Name of analysis pipeline to use.
Pipeline_2:
########## OTHER ##########
# Name of executing protocol for documentation
Program:
# Volume of hybmix in ul
Hybmix_volume: 500
# Temperature used for staining and washing
Staining_temperature: 37
# Temperature used for the readout probes
Readout_temperature: 22
# temperature used for the stripping
Stripping_temperature: 22
# Temperature used for heatshock
Heatshock_temperature: 22
# Temperature used for imaging
Imaging_temperature: 20
# Volume of all buffers in ul, Integer/float
Volumes:
RunningBuffer:
# Port 1-10 on acuator valve 1
P1:
P2:
P3:
P4:
P5:
P6:
P7:
P8:
P9:
P10:
# Port 1-10 on acuator valve 2 are numberd 11-20.
P11:
P12:
P13:
P14:
P15:
P16:
P17:
P18:
P19:
P20:
# Name of the buffer connected to the ports.
# Use "Waste" for the connection to the waste, "Valve2" for the connection to Valve 2
# and use HYBXX for the hybridization mixes where XX are a number, like HYB05 or HYB10.
Ports:
# Buffer connected to the Syringe pump
RunningBuffer:
# Port 1-10 on acuator valve 1
P1:
P2:
P3:
P4:
P5:
P6:
P7:
P8:
P9:
P10:
# Port 1-10 on acuator valve 2 are numberd 11-20
P11:
P12:
P13:
P14:
P15:
P16:
P17:
P18:
P19:
P20:
# To which Hybridization in which chamber does the HYB X port belong
# Use "C1" for Chamber1 and "C2" for Chamber2, then append a lower dash plus cycle number
# Like: "C1_01" for Chamber1 cycle 1 or "C2_14" for Chamber2 cycle 14
# Append an A or B if you want to use indirect labeling. A for encoding probes, B for detection probes.
# For indirect labeling use: "C1_01_A" for Chamber 1 cycle 1 hybridization 1 (encoding probes),
# "C2_14_B" for Chamber 2, cycle 14, hybridization 2 (detection probes)
Hybmix:
# Port 1-10 on acuator valve 1
P1:
P2:
P3:
P4:
P5:
P6:
P7:
P8:
P9:
P10:
# Port 1-10 on acuator valve 2 are numberd 11-20.
P11:
P12:
P13:
P14:
P15:
P16:
P17:
P18:
P19:
P20:
# Targets of each round
# Gene name, Background, polyA, Beads or Nuclei
Targets:
########## Chamber 1 ##########
Chamber1:
Hybridization01:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization02:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization03:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization04:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization05:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization06:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization07:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization08:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization09:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization10:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization11:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization12:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization13:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization14:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization15:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization16:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization17:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization18:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization19:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization20:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization21:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization22:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization23:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization24:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization25:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization26:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization27:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization28:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization29:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization30:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
########## Chamber 2 ##########
Chamber2:
Hybridization01:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization02:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization03:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization04:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization05:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization06:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization07:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization08:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization09:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization10:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization11:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization12:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization13:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization14:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization15:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization16:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization17:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization18:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization19:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization20:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization21:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization22:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization23:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization24:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization25:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization26:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization27:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization28:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization29:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
Hybridization30:
DAPI:
Atto425:
FITC:
Cy3:
TxRed:
Cy5:
Cy7:
QDot:
BrightField:
Europium:
# Table with active/connected Machines. Set to 1 for all used machines.
#If you switch off a machine set the value below to zero. Then the machine will not be checked for errors anymore.
Machines:
CavroXE1000: 0
CavroXCalibur: 1
MXValve1: 1
MXValve2: 1
Degassi: None
ThermoCube1: 0
ThermoCube2: 0
Oasis1: 0
Oasis2: 0
YoctoThermistor: 0
TC720: 1
#Put the identifiers of each machine here. This will be used to find the USB port for each device.
#Find the ports using the "find_address()" Function, then paste the device serial number here.
#This is the safest method.
Machine_identification:
CavroXE1000: #not needed
CavroXCalibur: #not needed
MXValve1:
MXValve2:
ThermoCube1:
ThermoCube2:
Oasis1:
Oasis2:
YoctoThermistor:
TC720:
#If the identifier can not be found, you can use a fixed USB port.
#Find the device address using the "find_address()" function and put it below.
#On Windows it is formatted as: "COMX" where X is a number.
#On Linuxt it is formatted as: "/dev/ttyUSBX" where X is a number.
#This method works only if the cabels are not moved, use with caution.
Fixed_USB_port:
CavroXE1000:
CavroXCalibur:
MXValve1:
MXValve2:
ThermoCube1:
ThermoCube2:
Oasis1:
Oasis2:
YoctoThermistor:
TC720:
#Pushbullet access tokens used for sending push messages to the user.
#Make an account on: https://www.pushbullet.com/, goto settings, create and add.
Operator_address:
operator1:
operator2:
operator3:
operator4:
operator5:
operator6:
operator7:
operator8:
operator9:
operator10:
# ul between the valve and the target component.
# For instance, to pump Hyb mix into the chamber the distance from the recevoir (valve) needs to be bridged.
# The volume of the tubes running from the valve to the chamber is called the padding volume.
# The pump will add the padding volume in SSC to the recevoir/syringe to push out so that all the Hyb mix reaches the
# Chamber without the tubes being filled with valuable Hyb mix.
Padding:
# Volume to the degasser
Degass:
# Port 1-10 on valve 1
P1:
P2:
P3:
P4:
P5:
P6:
P7:
P8:
P9:
P10:
# Port 1-10 on valve 2 are numberd 11-20.
# Measure full volume from the end of the recervoir on Valve1 to the target